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Nonrandomized Clinical sentence examples within Prospective Nonrandomized Clinical
Methods: A prospective nonrandomized clinical trial by the ECOG-ACRIN Cancer Research Group (E4112) enrolled women diagnosed with unilateral DCIS from 75 institutions between March 2015 and April 2016.
Methods: A prospective nonrandomized clinical trial by the ECOG-ACRIN Cancer Research Group (E4112) enrolled women diagnosed with unilateral DCIS from 75 institutions between March 2015 and April 2016.
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METHODS
In a prospective nonrandomized clinical trial, a total of 80 patients undergoing diagnostic CAG by TSA were divided into two equal groups: manual compression and mechanical compression (using radial TR band), the main end point of which was primary hemostasis time.
METHODS
In a prospective nonrandomized clinical trial, a total of 80 patients undergoing diagnostic CAG by TSA were divided into two equal groups: manual compression and mechanical compression (using radial TR band), the main end point of which was primary hemostasis time.
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Nonrandomized Clinical sentence examples within 1 Nonrandomized Clinical
Results: Four studies were included in the review (3 cross-sectional studies and 1 nonrandomized clinical trial).
Results: Four studies were included in the review (3 cross-sectional studies and 1 nonrandomized clinical trial).
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Design, Setting, and Participants
This single-center phase 1 nonrandomized clinical trial assessing an empirical CE-sparing technique enrolled patients from July 2015 to January 2019.
Design, Setting, and Participants
This single-center phase 1 nonrandomized clinical trial assessing an empirical CE-sparing technique enrolled patients from July 2015 to January 2019.
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Nonrandomized Clinical sentence examples within Label Nonrandomized Clinical
In this open‐label nonrandomized clinical trial, efficacy of nano‐curcumin oral formulation has been evaluated in hospitalized patients with mild–moderate COVID‐19.
In this open‐label nonrandomized clinical trial, efficacy of nano‐curcumin oral formulation has been evaluated in hospitalized patients with mild–moderate COVID‐19.
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Methods This open-label nonrandomized clinical trial evaluated 33 patients diagnosed with BKC.
Methods This open-label nonrandomized clinical trial evaluated 33 patients diagnosed with BKC.
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Nonrandomized Clinical sentence examples within 2 Nonrandomized Clinical
Design, Setting, and Participants
This 3-part, open-label, phase 1/2 nonrandomized clinical trial with dose-escalation/dose-expansion cohorts (28 sites in the US) and a single-arm extension cohort (EXCLAIM; 40 sites in Asia, Europe, and North America) was conducted between June 2016 and November 2020 (data cutoff date).
Design, Setting, and Participants
This 3-part, open-label, phase 1/2 nonrandomized clinical trial with dose-escalation/dose-expansion cohorts (28 sites in the US) and a single-arm extension cohort (EXCLAIM; 40 sites in Asia, Europe, and North America) was conducted between June 2016 and November 2020 (data cutoff date).
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Design, Setting, and Participants
Two parallel phase 2 nonrandomized clinical trials were conducted from November 11, 2016, to October 2, 2018, among 46 patients in Israel and Texas to determine the effectiveness of olaparib as monotherapy in advanced, previously treated PDAC with BRCAness.
Design, Setting, and Participants
Two parallel phase 2 nonrandomized clinical trials were conducted from November 11, 2016, to October 2, 2018, among 46 patients in Israel and Texas to determine the effectiveness of olaparib as monotherapy in advanced, previously treated PDAC with BRCAness.
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Nonrandomized Clinical sentence examples within Noncomparative Nonrandomized Clinical
Settings and design This is a prospective noncomparative nonrandomized clinical study that was carried out at Rooya Eye Center, Alexandria, Egypt.
Settings and design This is a prospective noncomparative nonrandomized clinical study that was carried out at Rooya Eye Center, Alexandria, Egypt.
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Setting and design This is a prospective noncomparative nonrandomized clinical study that was carried out at Alex Eye Center, Alexandria, Egypt.
Setting and design This is a prospective noncomparative nonrandomized clinical study that was carried out at Alex Eye Center, Alexandria, Egypt.
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Nonrandomized Clinical sentence examples within nonrandomized clinical trial
Results: Four studies were included in the review (3 cross-sectional studies and 1 nonrandomized clinical trial).
Results: Four studies were included in the review (3 cross-sectional studies and 1 nonrandomized clinical trial).
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Key Points Question Can the favorable properties of an ultrasmall fluorescent core-shell silica nanoparticle aid real-time image-guided detection, localization, and surgical management of sentinel lymph nodes (SLNs) in patients with head and neck melanoma? Findings In this nonrandomized clinical trial of 24 patients, real-time, particle-based fluorescence imaging of SLNs was feasible and safe at the microdosing level and enabled deep-tissue nodal detection.
Key Points Question Can the favorable properties of an ultrasmall fluorescent core-shell silica nanoparticle aid real-time image-guided detection, localization, and surgical management of sentinel lymph nodes (SLNs) in patients with head and neck melanoma? Findings In this nonrandomized clinical trial of 24 patients, real-time, particle-based fluorescence imaging of SLNs was feasible and safe at the microdosing level and enabled deep-tissue nodal detection.
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Nonrandomized Clinical sentence examples within nonrandomized clinical study
METHODS
This prospective comparative nonrandomized clinical study comprised 75 eyes (75 patients).
METHODS
This prospective comparative nonrandomized clinical study comprised 75 eyes (75 patients).
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Design, Setting, and Participants
This prospective, longitudinal, nonrandomized clinical study carried out in a single tertiary referral center (December 1, 2015, to July 1, 2017) included 2 groups of 30 patients.
Design, Setting, and Participants
This prospective, longitudinal, nonrandomized clinical study carried out in a single tertiary referral center (December 1, 2015, to July 1, 2017) included 2 groups of 30 patients.
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10.1097/MD.0000000000027311
Results: Four studies were included in the review (3 cross-sectional studies and 1 nonrandomized clinical trial).
Results: Four studies were included in the review (3 cross-sectional studies and 1 nonrandomized clinical trial).
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10.1001/jamanetworkopen.2021.1936
Key Points Question Can the favorable properties of an ultrasmall fluorescent core-shell silica nanoparticle aid real-time image-guided detection, localization, and surgical management of sentinel lymph nodes (SLNs) in patients with head and neck melanoma? Findings In this nonrandomized clinical trial of 24 patients, real-time, particle-based fluorescence imaging of SLNs was feasible and safe at the microdosing level and enabled deep-tissue nodal detection.
Key Points Question Can the favorable properties of an ultrasmall fluorescent core-shell silica nanoparticle aid real-time image-guided detection, localization, and surgical management of sentinel lymph nodes (SLNs) in patients with head and neck melanoma? Findings In this nonrandomized clinical trial of 24 patients, real-time, particle-based fluorescence imaging of SLNs was feasible and safe at the microdosing level and enabled deep-tissue nodal detection.
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10.1097/ACI.0000000000000743
Recent findings To date, there has been one multicenter, double-blind, randomized controlled trial of WOIT, one randomized, noncontrolled trial of WOIT, and several smaller, nonrandomized clinical trials of WOIT.
Recent findings To date, there has been one multicenter, double-blind, randomized controlled trial of WOIT, one randomized, noncontrolled trial of WOIT, and several smaller, nonrandomized clinical trials of WOIT.
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10.1016/j.ctcp.2021.101477
PubMed, Scopus, Cochrane Library, Physiotherapy Evidence Database, Embase, Web of Science, Cumulative Index to Nursing and Allied Health Literature Complete, and ProQuest Medical library were searched from their inception to April 1, 2021 for randomized or nonrandomized clinical trials published in English.
PubMed, Scopus, Cochrane Library, Physiotherapy Evidence Database, Embase, Web of Science, Cumulative Index to Nursing and Allied Health Literature Complete, and ProQuest Medical library were searched from their inception to April 1, 2021 for randomized or nonrandomized clinical trials published in English.
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10.14444/8046
Methods: This was a retrospective, nonrandomized clinical cohort investigation of patients with VCF and posterior wall disruption treated with BK between 2010 and 2018.
Methods: This was a retrospective, nonrandomized clinical cohort investigation of patients with VCF and posterior wall disruption treated with BK between 2010 and 2018.
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10.2174/1874210602115010151
English language study performed on humans, randomized or nonrandomized clinical trials, comparing the effect of fluoride and chlorhexidine varnish on WSL was included in the review.
English language study performed on humans, randomized or nonrandomized clinical trials, comparing the effect of fluoride and chlorhexidine varnish on WSL was included in the review.
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10.1172/jci.insight.146592
METHODS Two single-arm, prospective, nonrandomized clinical trials were conducted at the University of Pennsylvania from May 2017 to March 2020.
METHODS Two single-arm, prospective, nonrandomized clinical trials were conducted at the University of Pennsylvania from May 2017 to March 2020.
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10.4103/mmj.mmj_269_19
Patients and methods This is a nonrandomized clinical trial conducted on 40 Egyptian patients with AIS who were eligible for intravenous alteplase.
Patients and methods This is a nonrandomized clinical trial conducted on 40 Egyptian patients with AIS who were eligible for intravenous alteplase.
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10.1200/JCO.2021.39.15_SUPPL.6564
Methods: A prospective nonrandomized clinical trial by the ECOG-ACRIN Cancer Research Group (E4112) enrolled women diagnosed with unilateral DCIS from 75 institutions between March 2015 and April 2016.
Methods: A prospective nonrandomized clinical trial by the ECOG-ACRIN Cancer Research Group (E4112) enrolled women diagnosed with unilateral DCIS from 75 institutions between March 2015 and April 2016.
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10.1167/tvst.10.3.5
In this first nonrandomized clinical trial we assessed its safety and ability to reduce intraocular pressure (IOP).
In this first nonrandomized clinical trial we assessed its safety and ability to reduce intraocular pressure (IOP).
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10.1001/jamaoncol.2021.4761
Design, Setting, and Participants
This 3-part, open-label, phase 1/2 nonrandomized clinical trial with dose-escalation/dose-expansion cohorts (28 sites in the US) and a single-arm extension cohort (EXCLAIM; 40 sites in Asia, Europe, and North America) was conducted between June 2016 and November 2020 (data cutoff date).
Design, Setting, and Participants
This 3-part, open-label, phase 1/2 nonrandomized clinical trial with dose-escalation/dose-expansion cohorts (28 sites in the US) and a single-arm extension cohort (EXCLAIM; 40 sites in Asia, Europe, and North America) was conducted between June 2016 and November 2020 (data cutoff date).
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10.1007/s43440-021-00225-3
Randomized or nonrandomized clinical trials and retrospective or prospective-controlled longitudinal studies were screened for this systematic review.
Randomized or nonrandomized clinical trials and retrospective or prospective-controlled longitudinal studies were screened for this systematic review.
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10.1016/j.clml.2021.01.013
We proposed a phase 2, open, prospective, multicenter, nonrandomized clinical trial for the adoptive infusion of haploidentical K562-mb15-41BBL-activated and expanded NK (NKAE) cells as a consolidation strategy for children with favorable and intermediate risk AML in first complete remission after chemotherapy (NCT02763475).
We proposed a phase 2, open, prospective, multicenter, nonrandomized clinical trial for the adoptive infusion of haploidentical K562-mb15-41BBL-activated and expanded NK (NKAE) cells as a consolidation strategy for children with favorable and intermediate risk AML in first complete remission after chemotherapy (NCT02763475).
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10.3390/jcm10102162
Through a nonrandomized clinical trial, we evaluated the effect of the combination of hysteroscopic endometrial injury and the freeze-all technique on pregnancy parameters in a cohort of RIF patients; (2) Methods: The study group comprised of 30 patients with RIF that underwent a hysteroscopic endometrial injury prior to a frozen embryo transfer cycle; another 30 patients with RIF, comprising the control group, underwent a standard frozen cycle with no adjuvant treatment before.
Through a nonrandomized clinical trial, we evaluated the effect of the combination of hysteroscopic endometrial injury and the freeze-all technique on pregnancy parameters in a cohort of RIF patients; (2) Methods: The study group comprised of 30 patients with RIF that underwent a hysteroscopic endometrial injury prior to a frozen embryo transfer cycle; another 30 patients with RIF, comprising the control group, underwent a standard frozen cycle with no adjuvant treatment before.
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10.1093/noajnl/vdaa146
Conclusions Our newly devised long-term survival-predictive nomogram based on clinical and genomic data can be used to advise patients regarding their potential outcomes and account for confounding factors in nonrandomized clinical trials.
Conclusions Our newly devised long-term survival-predictive nomogram based on clinical and genomic data can be used to advise patients regarding their potential outcomes and account for confounding factors in nonrandomized clinical trials.
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10.1001/jamaoncol.2021.2086
Conclusions and Relevance
In this phase 1b/2a nonrandomized clinical trial, type I and type II KIT inhibitors PLX9486 and sunitinib were safely coadministered at the recommended dose of both single agents in patients with refractory GIST.
Conclusions and Relevance
In this phase 1b/2a nonrandomized clinical trial, type I and type II KIT inhibitors PLX9486 and sunitinib were safely coadministered at the recommended dose of both single agents in patients with refractory GIST.
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10.22141/2663-3272.4.1.2021.229866
We conducted a literature review that included randomized and nonrandomized clinical trials from 2010 to 2020.
We conducted a literature review that included randomized and nonrandomized clinical trials from 2010 to 2020.
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10.18240/ijo.2021.02.16
METHODS
This prospective comparative nonrandomized clinical study comprised 75 eyes (75 patients).
METHODS
This prospective comparative nonrandomized clinical study comprised 75 eyes (75 patients).
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10.4103/jispcd.JISPCD_109_21
Data from all randomized and nonrandomized clinical trials, cross-sectional studies, case-control, cohort studies, literature, and systematic reviews were included.
Data from all randomized and nonrandomized clinical trials, cross-sectional studies, case-control, cohort studies, literature, and systematic reviews were included.
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10.1002/ptr.7004
In this open‐label nonrandomized clinical trial, efficacy of nano‐curcumin oral formulation has been evaluated in hospitalized patients with mild–moderate COVID‐19.
In this open‐label nonrandomized clinical trial, efficacy of nano‐curcumin oral formulation has been evaluated in hospitalized patients with mild–moderate COVID‐19.
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10.1111/jocd.14135
METHODS
A research was done using PubMed database on 12 april 2020 in order to retrieve all case reports, case series, cohort studies, randomized and nonrandomized clinical trials were included describing FFD among patients.
METHODS
A research was done using PubMed database on 12 april 2020 in order to retrieve all case reports, case series, cohort studies, randomized and nonrandomized clinical trials were included describing FFD among patients.
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10.21037/AOJ-20-62
Three small, nonrandomized clinical trials have examined nonsurgical adjunct approaches to prevent contractures after fracture-dislocations or recurrence of contractures after operative releases of established contractures.
Three small, nonrandomized clinical trials have examined nonsurgical adjunct approaches to prevent contractures after fracture-dislocations or recurrence of contractures after operative releases of established contractures.
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10.1002/sctm.20-0369
In a nonrandomized clinical trial, we imaged 37 patients with stroke: 17 patients treated with MNCs (treated) and 20 patients who received standard of care (nontreated) at 1, 3, and 12 months onset of stroke on 3.
In a nonrandomized clinical trial, we imaged 37 patients with stroke: 17 patients treated with MNCs (treated) and 20 patients who received standard of care (nontreated) at 1, 3, and 12 months onset of stroke on 3.
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10.1053/j.jvca.2021.07.033
DESIGN
A prospective, nonrandomized clinical investigation.
DESIGN
A prospective, nonrandomized clinical investigation.
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10.1016/j.jen.2021.10.001
Methods
A nonrandomized clinical trial was performed.
Methods
A nonrandomized clinical trial was performed.
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10.14744/anatoljcardiol.2020.99672
METHODS
In a prospective nonrandomized clinical trial, a total of 80 patients undergoing diagnostic CAG by TSA were divided into two equal groups: manual compression and mechanical compression (using radial TR band), the main end point of which was primary hemostasis time.
METHODS
In a prospective nonrandomized clinical trial, a total of 80 patients undergoing diagnostic CAG by TSA were divided into two equal groups: manual compression and mechanical compression (using radial TR band), the main end point of which was primary hemostasis time.
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10.1001/jamaoncol.2021.0611
Conclusions and Relevance
In this nonrandomized clinical trial, carfilzomib-lenalidomide-dexamethasone-daratumumab combination therapy was associated with high rates of MRD negativity in patients with newly diagnosed multiple myeloma and high rates of PFS.
Conclusions and Relevance
In this nonrandomized clinical trial, carfilzomib-lenalidomide-dexamethasone-daratumumab combination therapy was associated with high rates of MRD negativity in patients with newly diagnosed multiple myeloma and high rates of PFS.
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10.1016/j.surg.2020.12.008
METHODS
A thorough PubMed search was conducted to identify randomized clinical trials and nonrandomized clinical trials with ≥100 patients.
METHODS
A thorough PubMed search was conducted to identify randomized clinical trials and nonrandomized clinical trials with ≥100 patients.
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10.1001/jamanetworkopen.2021.22826
Key Points Question Are audit and feedback strategies and educational outreach associated with clinician perceptions of the feasibility, acceptability, appropriateness, and safety of continuous pulse oximetry use in children hospitalized with bronchiolitis who are not receiving supplemental oxygen (guideline-discordant use)? Findings In this 6-hospital single-group nonrandomized clinical trial, 847 nurses and physicians highly rated the feasibility, acceptability, and appropriateness of audit and feedback strategies and educational outreach.
Key Points Question Are audit and feedback strategies and educational outreach associated with clinician perceptions of the feasibility, acceptability, appropriateness, and safety of continuous pulse oximetry use in children hospitalized with bronchiolitis who are not receiving supplemental oxygen (guideline-discordant use)? Findings In this 6-hospital single-group nonrandomized clinical trial, 847 nurses and physicians highly rated the feasibility, acceptability, and appropriateness of audit and feedback strategies and educational outreach.
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10.1001/jamaoto.2021.0327
Design, Setting, and Participants
This prospective, longitudinal, nonrandomized clinical study carried out in a single tertiary referral center (December 1, 2015, to July 1, 2017) included 2 groups of 30 patients.
Design, Setting, and Participants
This prospective, longitudinal, nonrandomized clinical study carried out in a single tertiary referral center (December 1, 2015, to July 1, 2017) included 2 groups of 30 patients.
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10.1093/jncics/pkab012
Methods We performed a systematic search of MEDLINE, EMBASE, and conference proceedings up to December 2019 for randomized and nonrandomized clinical trials of anti-PD-1 or anti-PD-L1 monotherapy in metastatic non-small cell lung cancer.
Methods We performed a systematic search of MEDLINE, EMBASE, and conference proceedings up to December 2019 for randomized and nonrandomized clinical trials of anti-PD-1 or anti-PD-L1 monotherapy in metastatic non-small cell lung cancer.
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10.1001/jamaoncol.2021.0281
Design, Setting, and Participants
This single-center phase 1 nonrandomized clinical trial assessing an empirical CE-sparing technique enrolled patients from July 2015 to January 2019.
Design, Setting, and Participants
This single-center phase 1 nonrandomized clinical trial assessing an empirical CE-sparing technique enrolled patients from July 2015 to January 2019.
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10.37897/rjn.2021.2.13
This single-center, prospective, controlled, nonrandomized clinical trial included 96 children aged 2 to 10 years with autism spectrum disorders associated with a genetic folate deficiency (study group, SG).
This single-center, prospective, controlled, nonrandomized clinical trial included 96 children aged 2 to 10 years with autism spectrum disorders associated with a genetic folate deficiency (study group, SG).
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10.1155/2021/6664864
Methods In this nonrandomized clinical trial, eighteen hEDS patients (4 males and 14 females) with mean age 21 years (range 13-55) were recruited and evaluated before and after three months of rehabilitation treatment.
Methods In this nonrandomized clinical trial, eighteen hEDS patients (4 males and 14 females) with mean age 21 years (range 13-55) were recruited and evaluated before and after three months of rehabilitation treatment.
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10.18502/ijhoscr.v15i1.5248
Materials and Methods: Sixty-six patients with acute lymphoblastic leukemia undergoing chemotherapy along with their caregivers participated in this nonrandomized clinical trial.
Materials and Methods: Sixty-six patients with acute lymphoblastic leukemia undergoing chemotherapy along with their caregivers participated in this nonrandomized clinical trial.
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10.4103/JRMS.JRMS_25_20
Materials and Methods: The study was a nonrandomized clinical trial conducted in Tehran, Iran, from July 2019 to January 2020.
Materials and Methods: The study was a nonrandomized clinical trial conducted in Tehran, Iran, from July 2019 to January 2020.
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10.1016/j.imr.2021.100801
Results
: In this scoping review, 16 research articles were included: 7 case reports, 6 observational studies, 1 review, 1 RCT and 1 nonrandomized clinical trial.
Results
: In this scoping review, 16 research articles were included: 7 case reports, 6 observational studies, 1 review, 1 RCT and 1 nonrandomized clinical trial.
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10.1097/WON.0000000000000779
DESIGN: A prospective, nonrandomized clinical trial.
DESIGN: A prospective, nonrandomized clinical trial.
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10.4103/DJO.DJO_47_20
Settings and design This is a prospective noncomparative nonrandomized clinical study that was carried out at Rooya Eye Center, Alexandria, Egypt.
Settings and design This is a prospective noncomparative nonrandomized clinical study that was carried out at Rooya Eye Center, Alexandria, Egypt.
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10.4103/DJO.DJO_48_20
Setting and design This is a prospective noncomparative nonrandomized clinical study that was carried out at Alex Eye Center, Alexandria, Egypt.
Setting and design This is a prospective noncomparative nonrandomized clinical study that was carried out at Alex Eye Center, Alexandria, Egypt.
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10.4103/jisppd.jisppd_487_20
Materials and Method: This nonrandomized clinical trial is comprised of two parts.
Materials and Method: This nonrandomized clinical trial is comprised of two parts.
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10.22038/RCM.2021.55887.1356
Nonrandomized clinical trials or those without a control group were excluded from the present study.
Nonrandomized clinical trials or those without a control group were excluded from the present study.
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10.1001/jamaoncol.2021.0006
Design, Setting, and Participants
Two parallel phase 2 nonrandomized clinical trials were conducted from November 11, 2016, to October 2, 2018, among 46 patients in Israel and Texas to determine the effectiveness of olaparib as monotherapy in advanced, previously treated PDAC with BRCAness.
Design, Setting, and Participants
Two parallel phase 2 nonrandomized clinical trials were conducted from November 11, 2016, to October 2, 2018, among 46 patients in Israel and Texas to determine the effectiveness of olaparib as monotherapy in advanced, previously treated PDAC with BRCAness.
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10.32098/MLTJ.02.2018.03
Methods: Nonrandomized clinical trial of 24 patients with R/CT divided into nonsmoking (n=12) and smoking (n=12) groups, which received physical therapy three times a week for four weeks.
Methods: Nonrandomized clinical trial of 24 patients with R/CT divided into nonsmoking (n=12) and smoking (n=12) groups, which received physical therapy three times a week for four weeks.
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10.1016/J.DOMANIEND.2019.01.008
The study design was a nonrandomized clinical trial.
The study design was a nonrandomized clinical trial.
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10.1001/jamaoncol.2018.6269
Design, Setting, and Participants
Analysis of a prospective, cohort, nonrandomized clinical trial that enrolled women with DCIS on core biopsy who were candidates for wide local excision (WLE) from 75 institutions from March 25, 2015, to April 27, 2016, through the Eastern Cooperative Oncology Group-American College of Radiology Imaging Network trial E4112.
Design, Setting, and Participants
Analysis of a prospective, cohort, nonrandomized clinical trial that enrolled women with DCIS on core biopsy who were candidates for wide local excision (WLE) from 75 institutions from March 25, 2015, to April 27, 2016, through the Eastern Cooperative Oncology Group-American College of Radiology Imaging Network trial E4112.
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10.12816/EJHM.2019.32062
Patients and Methods: this study was a prospective, follow-up nonrandomized clinical trial, carried out on 50 eyes with ACG.
Patients and Methods: this study was a prospective, follow-up nonrandomized clinical trial, carried out on 50 eyes with ACG.
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10.12816/EJHM.2019.23566
Patients and methods: A prospective nonrandomized clinical comparative study.
Patients and methods: A prospective nonrandomized clinical comparative study.
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10.1055/s-0039-1695677
Study Design This was a nonrandomized clinical trial.
Study Design This was a nonrandomized clinical trial.
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10.1213/ANE.0000000000004047
METHODS
In this nonrandomized clinical trial, an IV infusion of 3 mL/kg of 20% albumin was given at a constant rate during 30 minutes to 15 patients on the first day after major open abdominal surgery (mean operating time 5.
METHODS
In this nonrandomized clinical trial, an IV infusion of 3 mL/kg of 20% albumin was given at a constant rate during 30 minutes to 15 patients on the first day after major open abdominal surgery (mean operating time 5.
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10.21608/ESJ.2019.10129.1092
Study Design: A prospective, nonrandomized clinical controlled trial.
Study Design: A prospective, nonrandomized clinical controlled trial.
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10.1016/J.SOARD.2019.04.022
METHODS
The present study is a nonrandomized clinical series describing our preliminary results using a transgastric inserted single-port device for ERCP after RYGB.
METHODS
The present study is a nonrandomized clinical series describing our preliminary results using a transgastric inserted single-port device for ERCP after RYGB.
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10.1097/PRA.0000000000000353
It is important to note that most of the data are based on preclinical studies and nonrandomized clinical trials with relatively small sample sizes, so that it is not possible to draw unequivocal conclusions with regard to the clinical relevance of the findings.
It is important to note that most of the data are based on preclinical studies and nonrandomized clinical trials with relatively small sample sizes, so that it is not possible to draw unequivocal conclusions with regard to the clinical relevance of the findings.
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10.1016/J.OOOO.2019.02.014
Eligibility criteria included randomized and nonrandomized clinical trials, prospective or retrospective cohorts, case controls, and case series evaluating the association between biomarkers and MRONJ.
Eligibility criteria included randomized and nonrandomized clinical trials, prospective or retrospective cohorts, case controls, and case series evaluating the association between biomarkers and MRONJ.
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10.21608/mjcu.2019.65641
Patients and Methods: This is a retrospective nonrandomized clinical and angiographic study of all ten patients with paragangliomas who undergone pre-operative embolization in Department of Neurosurgery-Tanta University between 2010 and 2016.
Patients and Methods: This is a retrospective nonrandomized clinical and angiographic study of all ten patients with paragangliomas who undergone pre-operative embolization in Department of Neurosurgery-Tanta University between 2010 and 2016.
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10.4103/ijdr.IJDR_779_17
Materials and Methods: An in vivo nonrandomized clinical trial study was carried among 60 children.
Materials and Methods: An in vivo nonrandomized clinical trial study was carried among 60 children.
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10.1093/advances/nmy125
A total of 9 studies consisting of 2 randomized parallel-arm trials, 4 crossover trials, and 3 nonrandomized clinical or surgical trials were included.
A total of 9 studies consisting of 2 randomized parallel-arm trials, 4 crossover trials, and 3 nonrandomized clinical or surgical trials were included.
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10.1016/J.BJPS.2019.04.013
METHODS
Randomized clinical trial (RCT) and nonrandomized clinical trial (NRCT) studies comparing AS to any other skin substitute in the treatment of burns were extracted from PubMed/Medline, Scopus, EMBASE, and Web of Science.
METHODS
Randomized clinical trial (RCT) and nonrandomized clinical trial (NRCT) studies comparing AS to any other skin substitute in the treatment of burns were extracted from PubMed/Medline, Scopus, EMBASE, and Web of Science.
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10.1097/DSS.0000000000002020
All randomized and nonrandomized clinical trials, case cohorts, case reports, and case series were included with the exception of 2 studies, which were excluded due to unavailability.
All randomized and nonrandomized clinical trials, case cohorts, case reports, and case series were included with the exception of 2 studies, which were excluded due to unavailability.
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10.1155/2019/3143469
Methods This open-label nonrandomized clinical trial evaluated 33 patients diagnosed with BKC.
Methods This open-label nonrandomized clinical trial evaluated 33 patients diagnosed with BKC.
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10.1093/infdis/jiy465
Methods Follow-up of a nonrandomized clinical trial to evaluate the 5-year antibody persistence of the bHPV in girls (age, 9–10 years) and women (age, 18–24 years).
Methods Follow-up of a nonrandomized clinical trial to evaluate the 5-year antibody persistence of the bHPV in girls (age, 9–10 years) and women (age, 18–24 years).
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10.1016/j.annemergmed.2018.11.011
Methods: This was a secondary analysis of a nonrandomized clinical trial with concurrent controls, conducted at 5 pediatric and 8 general EDs between November 2011 and June 2014, enrolling patients younger than 18 years who had minor blunt head trauma.
Methods: This was a secondary analysis of a nonrandomized clinical trial with concurrent controls, conducted at 5 pediatric and 8 general EDs between November 2011 and June 2014, enrolling patients younger than 18 years who had minor blunt head trauma.
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10.3906/sag-1708-112
Materials and methods In this prospective nonrandomized clinical trial, 21 patients were treated with endoscopic or conventional CST between 2012 and 2016.
Materials and methods In this prospective nonrandomized clinical trial, 21 patients were treated with endoscopic or conventional CST between 2012 and 2016.
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10.5888/pcd16.190156
Methods We conducted a nonrandomized clinical trial with matched controls.
Methods We conducted a nonrandomized clinical trial with matched controls.
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10.1155/2019/3561857
Study design A prospective nonrandomized clinical study.
Study design A prospective nonrandomized clinical study.
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10.3390/dj7010015
Related English-language articles published since 2000 to 2017, including reviews, meta-analyses, and original papers (randomized or nonrandomized clinical trials; prospective or retrospective cohort studies), case reports, and case series about oral diseases were appraised.
Related English-language articles published since 2000 to 2017, including reviews, meta-analyses, and original papers (randomized or nonrandomized clinical trials; prospective or retrospective cohort studies), case reports, and case series about oral diseases were appraised.
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10.1159/000495153
Patients and Methods: This prospective nonrandomized clinical study included 33 male patients aged 18–75 years hospitalized for primary inguinal hernia repair surgery.
Patients and Methods: This prospective nonrandomized clinical study included 33 male patients aged 18–75 years hospitalized for primary inguinal hernia repair surgery.
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10.4103/ijp.IJP_230_16
MATERIALS AND METHODS: The data were collected from a prospective, nonrandomized clinical study in healthy volunteers and patients with mild-moderate hepatic dysfunction and renal dysfunction.
MATERIALS AND METHODS: The data were collected from a prospective, nonrandomized clinical study in healthy volunteers and patients with mild-moderate hepatic dysfunction and renal dysfunction.
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