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Our aim is to evaluate its effectiveness in a national randomized-controlled clinical trial comparing iCBT-I to a waiting-list control condition at 3 and 6 months ( n = 70).
Our aim is to evaluate its effectiveness in a national randomized-controlled clinical trial comparing iCBT-I to a waiting-list control condition at 3 and 6 months ( n = 70).
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Our aim is to evaluate its effectiveness in a national randomized-controlled clinical trial comparing iCBT-I to a waiting-list control condition at 3 and 6 months ( n =70).
Our aim is to evaluate its effectiveness in a national randomized-controlled clinical trial comparing iCBT-I to a waiting-list control condition at 3 and 6 months ( n =70).
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10.1093/cdn/nzab010
Methods This was a secondary analysis of baseline data collected from a randomized-controlled clinical trial.
Methods This was a secondary analysis of baseline data collected from a randomized-controlled clinical trial.
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10.1093/ehjcvp/pvab016
METHODS AND RESULTS
This study was an analysis of serial magnetic resonance imaging (MRI) and circulating biomarker data acquired from patients with HER2-positive early stage breast cancer participating in a randomized-controlled clinical trial for the pharmaco-prevention of trastuzumab-associated cardiotoxicity.
METHODS AND RESULTS
This study was an analysis of serial magnetic resonance imaging (MRI) and circulating biomarker data acquired from patients with HER2-positive early stage breast cancer participating in a randomized-controlled clinical trial for the pharmaco-prevention of trastuzumab-associated cardiotoxicity.
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10.1016/j.jebdp.2021.101584
In this randomized-controlled clinical trial, studied group comprised laboratory-confirmed COVID-19 positive patients through nasopharyngeal swabs.
In this randomized-controlled clinical trial, studied group comprised laboratory-confirmed COVID-19 positive patients through nasopharyngeal swabs.
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10.1186/s13063-021-05263-z
Our aim is to evaluate its effectiveness in a national randomized-controlled clinical trial comparing iCBT-I to a waiting-list control condition at 3 and 6 months ( n = 70).
Our aim is to evaluate its effectiveness in a national randomized-controlled clinical trial comparing iCBT-I to a waiting-list control condition at 3 and 6 months ( n = 70).
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10.1089/g4h.2020.0165
Conclusion: The results support the efficacy and feasibility of using the videogame to promote active aging, and they encourage further evaluation through a randomized-controlled clinical trial.
Conclusion: The results support the efficacy and feasibility of using the videogame to promote active aging, and they encourage further evaluation through a randomized-controlled clinical trial.
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10.1007/82_2021_239
The traditional regulatory pathway for the evaluation of new vaccine candidates generally proceeds from preclinical through three successive phases of human trials, and the demonstration of efficacy is usually done through randomized-controlled clinical trials.
The traditional regulatory pathway for the evaluation of new vaccine candidates generally proceeds from preclinical through three successive phases of human trials, and the demonstration of efficacy is usually done through randomized-controlled clinical trials.
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10.1101/2021.03.07.21252302
In this randomized-controlled clinical trial, studied group comprised laboratory-confirmed COVID-19 positive patients through nasopharyngeal swabs.
In this randomized-controlled clinical trial, studied group comprised laboratory-confirmed COVID-19 positive patients through nasopharyngeal swabs.
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10.1007/s40520-021-01921-z
We conducted a double-blind randomized-controlled clinical study with 49 participants divided into two groups: one given 300 mg/day of magnesium citrate (n = 25) and the other one sachet/day of a placebo (n = 24).
We conducted a double-blind randomized-controlled clinical study with 49 participants divided into two groups: one given 300 mg/day of magnesium citrate (n = 25) and the other one sachet/day of a placebo (n = 24).
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10.1200/JCO.2021.39.15_SUPPL.E16522
Results: We identified 24 studies from inception to March 2020; among them 17 were peer reviewed and 7 were only reported as abstracts in national or international meetings, including a phase 3, randomized-controlled clinical trial.
Results: We identified 24 studies from inception to March 2020; among them 17 were peer reviewed and 7 were only reported as abstracts in national or international meetings, including a phase 3, randomized-controlled clinical trial.
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10.1101/2021.03.10.21252757
The relationship between these network changes and clinical improvements in balance and amelioration of ataxia after participation in the TBP requires a larger randomized-controlled clinical trial of the TBP in persons with RRMS.
The relationship between these network changes and clinical improvements in balance and amelioration of ataxia after participation in the TBP requires a larger randomized-controlled clinical trial of the TBP in persons with RRMS.
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10.2334/josnusd.20-0515
A split-mouth single-blind randomized-controlled clinical trial study was designed to investigate the effect of local and systemic vitamin C administration on extraction wound healing.
A split-mouth single-blind randomized-controlled clinical trial study was designed to investigate the effect of local and systemic vitamin C administration on extraction wound healing.
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10.1089/acm.2020.0531
Methods: In this prospective, randomized-controlled clinical trial, 80 patients with gastrointestinal cancer undergoing chemotherapy and at high risk for depression were randomized to an intervention group or a control group.
Methods: In this prospective, randomized-controlled clinical trial, 80 patients with gastrointestinal cancer undergoing chemotherapy and at high risk for depression were randomized to an intervention group or a control group.
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10.1101/2021.02.16.21251872
Here, we conducted a randomized-controlled clinical trial to determine the effectiveness and safety of probiotic supplements on antipsychotic-induced metabolic disturbance and weight gain.
Here, we conducted a randomized-controlled clinical trial to determine the effectiveness and safety of probiotic supplements on antipsychotic-induced metabolic disturbance and weight gain.
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10.1089/lrb.2019.0061
We conducted a randomized-controlled clinical study as well as in vitro experiments to investigate the efficacy and safety of far infrared radiation (FIR) to treat lymphedema in patients having previously undergone surgery for gynecological tumors.
We conducted a randomized-controlled clinical study as well as in vitro experiments to investigate the efficacy and safety of far infrared radiation (FIR) to treat lymphedema in patients having previously undergone surgery for gynecological tumors.
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10.21203/RS.3.RS-65491/V1
Our aim is to evaluate its effectiveness in a national randomized-controlled clinical trial comparing iCBT-I to a waiting-list control condition at 3 and 6 months ( n =70).
Our aim is to evaluate its effectiveness in a national randomized-controlled clinical trial comparing iCBT-I to a waiting-list control condition at 3 and 6 months ( n =70).
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10.1016/j.jns.2020.117224
We performed a systematic search in MEDLINE and SCOPUS databases on October 24, 2019 to identify all cohorts from randomized-controlled clinical trials or observational studies reporting on CMB prevalence and statin use.
We performed a systematic search in MEDLINE and SCOPUS databases on October 24, 2019 to identify all cohorts from randomized-controlled clinical trials or observational studies reporting on CMB prevalence and statin use.
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10.21203/rs.3.rs-731005/v1
Conclusion131I-MIBG treatment is effective on clinical outcomes in relapsed or refractory neuroblastoma, more randomized-controlled clinical trials investigating the efficacy of 131I-MIBG in combination with chemotherapy should be conducted.
Conclusion131I-MIBG treatment is effective on clinical outcomes in relapsed or refractory neuroblastoma, more randomized-controlled clinical trials investigating the efficacy of 131I-MIBG in combination with chemotherapy should be conducted.
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10.5606/ehc.2021.78393
Patients and methods This double-blind, prospective, randomized-controlled clinical study included a total of 90 patients (42 males, 48 females; mean age: 55.
Patients and methods This double-blind, prospective, randomized-controlled clinical study included a total of 90 patients (42 males, 48 females; mean age: 55.
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10.1161/STROKEAHA.120.030960
We aimed to evaluate the safety and efficacy of sonothrombolysis in patients with AIS with large vessel occlusion, by analyzing individual patient data of available randomized-controlled clinical trials.
We aimed to evaluate the safety and efficacy of sonothrombolysis in patients with AIS with large vessel occlusion, by analyzing individual patient data of available randomized-controlled clinical trials.
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10.21608/ejhm.2021.178619
Patients and Methods: Randomized-controlled clinical study included 24 patients with provox voice prosthesis rehabilitation 12 had primary tracheoesophageal puncture and 12 had secondary tracheoesophageal puncture.
Patients and Methods: Randomized-controlled clinical study included 24 patients with provox voice prosthesis rehabilitation 12 had primary tracheoesophageal puncture and 12 had secondary tracheoesophageal puncture.
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10.5606/TFTRD.2019.2534
Patients and methods
This randomized-controlled clinical trial included a total of 40 patients with PFPS (20 males, 20 females; mean age 46.
Patients and methods
This randomized-controlled clinical trial included a total of 40 patients with PFPS (20 males, 20 females; mean age 46.
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10.1016/j.psychres.2019.01.092
We examined the relationship of self- and clinician-rated Y-BOCS scores in participants with obsessive-compulsive disorder in pre (N = 128), post, (4 weeks, n = 104) and follow-up (6 months, n = 98) assessments of a randomized-controlled clinical trial.
We examined the relationship of self- and clinician-rated Y-BOCS scores in participants with obsessive-compulsive disorder in pre (N = 128), post, (4 weeks, n = 104) and follow-up (6 months, n = 98) assessments of a randomized-controlled clinical trial.
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10.1080/10503307.2017.1397796
To study the effects of fostering EP in psychotherapy for depression, this randomized-controlled clinical trial compares the efficacy and pattern of change of a cognitive–behavioral therapy that integrates emotion-focused techniques within an exposure framework (Exposure-Based Cognitive Therapy for depression; EBCT-R) to a standard cognitive–behavioral therapy (CBT).
To study the effects of fostering EP in psychotherapy for depression, this randomized-controlled clinical trial compares the efficacy and pattern of change of a cognitive–behavioral therapy that integrates emotion-focused techniques within an exposure framework (Exposure-Based Cognitive Therapy for depression; EBCT-R) to a standard cognitive–behavioral therapy (CBT).
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10.1097/01.JU.0000556282.95904.40
INTRODUCTION AND OBJECTIVES: The study was aimed to provide a prospective, long-term, randomized-controlled clinical comparison between the bipolar plasma vaporization of the prostate (BPVP), bipolar transurethral resection in saline (TURis) and monopolar transurethral resection of the prostate (TURP) in medium size benign prostatic hyperplasia (BPH) cases.
INTRODUCTION AND OBJECTIVES: The study was aimed to provide a prospective, long-term, randomized-controlled clinical comparison between the bipolar plasma vaporization of the prostate (BPVP), bipolar transurethral resection in saline (TURis) and monopolar transurethral resection of the prostate (TURP) in medium size benign prostatic hyperplasia (BPH) cases.
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10.1097/MD.0000000000017399
Methods: This is a randomized-controlled clinical study including patients from an urban tertiary hospital and a semi-urban community center, with a between-group, repeated-measures, longitudinal design.
Methods: This is a randomized-controlled clinical study including patients from an urban tertiary hospital and a semi-urban community center, with a between-group, repeated-measures, longitudinal design.
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10.1371/journal.pone.0219781
We included Cochrane Systematic Reviews and non-Cochrane Systematic Reviews of randomized-controlled clinical trials and not-randomized clinical trials, in all types of stroke, comparing the effects of interventions, control interventions and no interventions on balance-related outcomes.
We included Cochrane Systematic Reviews and non-Cochrane Systematic Reviews of randomized-controlled clinical trials and not-randomized clinical trials, in all types of stroke, comparing the effects of interventions, control interventions and no interventions on balance-related outcomes.
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10.5812/compreped.90011
Methods: In a randomized-controlled clinical trial in 2016, 90 term icteric neonates were divided into groups of 30.
Methods: In a randomized-controlled clinical trial in 2016, 90 term icteric neonates were divided into groups of 30.
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10.11588/heidok.00026124
Analyses relied on data from a randomized-controlled clinical trial which compared CBASP to SP in the treatment of 268 early-onset persistently depressed outpatients.
Analyses relied on data from a randomized-controlled clinical trial which compared CBASP to SP in the treatment of 268 early-onset persistently depressed outpatients.
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10.5853/jos.2018.02369
Future randomized-controlled clinical trials will provide definitive data on the aforementioned association.
Future randomized-controlled clinical trials will provide definitive data on the aforementioned association.
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10.1093/cdn/nzz031.FS15-08-19
Methods
Forty veterans with GWI are being recruited for a randomized-controlled clinical trial testing the effects of a low glutamate diet on neurological symptoms.
Methods
Forty veterans with GWI are being recruited for a randomized-controlled clinical trial testing the effects of a low glutamate diet on neurological symptoms.
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10.12659/MSM.912166
Material/Methods This was a prospective, open-label, randomized-controlled clinical trial.
Material/Methods This was a prospective, open-label, randomized-controlled clinical trial.
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10.3389/fpsyt.2019.00943
Only randomized-controlled clinical trials were included.
Only randomized-controlled clinical trials were included.
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10.1016/j.cptl.2019.09.011
The pre-assessment instructional activity was conducted the first week of each rotation; faculty members took turns working through a randomized-controlled clinical trial, highlighting and discussing key points based on their backgrounds and training.
The pre-assessment instructional activity was conducted the first week of each rotation; faculty members took turns working through a randomized-controlled clinical trial, highlighting and discussing key points based on their backgrounds and training.
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10.20540/jiaptr.2019.10.3.1823
Design: The study was an assessor-blinded and randomized-controlled clinical trial.
Design: The study was an assessor-blinded and randomized-controlled clinical trial.
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10.3390/nu11020228
In this randomized-controlled clinical trial, a total of 37 men and women between the ages of 65–80 were randomly assigned to consume 480 mL of tart cherry juice or control drink daily for 12 weeks.
In this randomized-controlled clinical trial, a total of 37 men and women between the ages of 65–80 were randomly assigned to consume 480 mL of tart cherry juice or control drink daily for 12 weeks.
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10.12659/MSM.913256
Material/Methods The meta-analysis was based on the participants, interventions, control, outcome (PICO) study design principle and 16 randomized-controlled clinical trials published from January 2000 to August 2018.
Material/Methods The meta-analysis was based on the participants, interventions, control, outcome (PICO) study design principle and 16 randomized-controlled clinical trials published from January 2000 to August 2018.
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