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Methods and Results:We selected 12 randomized controlled trials (n=131,978 patients) using PubMed and Embase (inception-June 1, 2018).
Methods and Results:We selected 12 randomized controlled trials (n=131,978 patients) using PubMed and Embase (inception-June 1, 2018).
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We screened the PubMed, EMBASE, Cochrane Library, China Science and Technology Journal, China National Knowledge Infrastructure, WANFANG, and China Biology Medicine disc databases and selected 12 randomized controlled trials involving a total of 1122 participants.
We screened the PubMed, EMBASE, Cochrane Library, China Science and Technology Journal, China National Knowledge Infrastructure, WANFANG, and China Biology Medicine disc databases and selected 12 randomized controlled trials involving a total of 1122 participants.
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The study, published in The Lancet, analyzed 12 randomized clinical trials involving 1041 participants followed up for a median of 1 year.
The study, published in The Lancet, analyzed 12 randomized clinical trials involving 1041 participants followed up for a median of 1 year.
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Methods: Using a defined selection criterion, a literature search identified 12 Randomized Clinical Trials (RCTs) involving 7,095 patients where CPIs have been used in the first-line setting.
Methods: Using a defined selection criterion, a literature search identified 12 Randomized Clinical Trials (RCTs) involving 7,095 patients where CPIs have been used in the first-line setting.
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10.1097/ANA.0000000000000644
Results: A total of 12 randomized controlled trials with 464 patients were eligible for inclusion in this analysis.
Results: A total of 12 randomized controlled trials with 464 patients were eligible for inclusion in this analysis.
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10.1007/s10877-019-00362-4
We identified 12 randomized controlled trials that compared one of five different nociception monitoring techniques to standard anesthesia care.
We identified 12 randomized controlled trials that compared one of five different nociception monitoring techniques to standard anesthesia care.
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10.1016/j.mayocp.2019.07.005
RESULTS
After a literature search and detailed evaluation, 12 randomized controlled trials with a total of 1539 individuals were included in the quantitative analysis.
RESULTS
After a literature search and detailed evaluation, 12 randomized controlled trials with a total of 1539 individuals were included in the quantitative analysis.
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10.1056/NEJM-JW.NA49889
This meta-analysis included 12 randomized trials.
This meta-analysis included 12 randomized trials.
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10.1093/ofid/ofz360.2438
Results 35 articles met inclusion criteria; 14 cross-sectional, 12 randomized trials, and 9 cohort studies, 25 articles had sufficient data for pooled analysis.
Results 35 articles met inclusion criteria; 14 cross-sectional, 12 randomized trials, and 9 cohort studies, 25 articles had sufficient data for pooled analysis.
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10.1016/j.rmed.2019.07.002
METHODS
Data were pooled from 12 randomized, placebo-controlled, parallel-group, Phase II or III trials from the global Boehringer Ingelheim program with once-daily tiotropium Respimat® (5 μg or 2.
METHODS
Data were pooled from 12 randomized, placebo-controlled, parallel-group, Phase II or III trials from the global Boehringer Ingelheim program with once-daily tiotropium Respimat® (5 μg or 2.
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10.1016/J.CHMED.2018.08.011
Results A total of 12 randomized controlled trials (RCTs) involving 829 patients were included.
Results A total of 12 randomized controlled trials (RCTs) involving 829 patients were included.
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10.1080/13607863.2019.1686457
Statistically significant results were reported in 8 of the 12 randomized controlled trials (RCTs).
Statistically significant results were reported in 8 of the 12 randomized controlled trials (RCTs).
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10.1080/10749357.2018.1550613
Results: Total of 12 randomized controlled trials were identified.
Results: Total of 12 randomized controlled trials were identified.
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10.1097/jnr.0000000000000363
RESULTS
Twenty-eight studies (13 cross-sectional, two longitudinal, 12 randomized controlled trial, and one retrospective chart review) fulfilled the inclusion criteria.
RESULTS
Twenty-eight studies (13 cross-sectional, two longitudinal, 12 randomized controlled trial, and one retrospective chart review) fulfilled the inclusion criteria.
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10.2147/DMSO.S188293
Results: We included 12 randomized controlled trials (RCTs) in the meta-analysis.
Results: We included 12 randomized controlled trials (RCTs) in the meta-analysis.
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10.3760/cma.j.issn.0376-2491.2019.30.010
Finally, 11 articles (12 randomized controlled trials) involving 1 629 hips or knees were included in this study.
Finally, 11 articles (12 randomized controlled trials) involving 1 629 hips or knees were included in this study.
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10.1253/circj.CJ-18-1321
Methods and Results:We selected 12 randomized controlled trials (n=131,978 patients) using PubMed and Embase (inception-June 1, 2018).
Methods and Results:We selected 12 randomized controlled trials (n=131,978 patients) using PubMed and Embase (inception-June 1, 2018).
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10.1024/0300-9831/a000577
The direct analysis included 96 works published between 2008 and 2018, including 12 randomized controlled trials and 23 systematic reviews and meta-analyses.
The direct analysis included 96 works published between 2008 and 2018, including 12 randomized controlled trials and 23 systematic reviews and meta-analyses.
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10.1016/j.tjog.2019.09.004
Finally, although 2277 articles were found to be related to misoprostol and oxytocin, only 12 randomized controlled (n = 6290) articles were included in the review.
Finally, although 2277 articles were found to be related to misoprostol and oxytocin, only 12 randomized controlled (n = 6290) articles were included in the review.
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10.14531/SS2019.3.8-16
The inclusion criteria was met by 65 publications: 33 systematic reviews, 12 randomized controlled studies, 19 multicenter studies; and one open prospective study was included in the review due to the particular treatment method used.
The inclusion criteria was met by 65 publications: 33 systematic reviews, 12 randomized controlled studies, 19 multicenter studies; and one open prospective study was included in the review due to the particular treatment method used.
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10.1136/tsaco-2018-000246
Results The study identified 12 randomized studies that included 1263 patients with isolated blunt and penetrating chest trauma.
Results The study identified 12 randomized studies that included 1263 patients with isolated blunt and penetrating chest trauma.
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10.1001/jama.2019.9142
The study, published in The Lancet, analyzed 12 randomized clinical trials involving 1041 participants followed up for a median of 1 year.
The study, published in The Lancet, analyzed 12 randomized clinical trials involving 1041 participants followed up for a median of 1 year.
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10.2217/fon-2018-0639
Results: A total of 12 randomized controlled trials (RCTs) with 6932 patients were included.
Results: A total of 12 randomized controlled trials (RCTs) with 6932 patients were included.
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10.1007/s10620-019-05896-w
Analysis of data from 12 randomized controlled trials with more than 1220 examinations challenges the usefulness of purgative preparation before small bowel VCE since it increases neither examination’s diagnostic yield [risk ratio 1.
Analysis of data from 12 randomized controlled trials with more than 1220 examinations challenges the usefulness of purgative preparation before small bowel VCE since it increases neither examination’s diagnostic yield [risk ratio 1.
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10.1097/MEG.0000000000001371
Results We included 12 randomized-controlled trials for analysis.
Results We included 12 randomized-controlled trials for analysis.
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10.4097/kja.19093
[5] evaluated a total of 312 randomized controlled trials published in the Journal of Anesthesiology between 2010 and 2017 analyzing Table 1 presented in each study.
[5] evaluated a total of 312 randomized controlled trials published in the Journal of Anesthesiology between 2010 and 2017 analyzing Table 1 presented in each study.
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10.4070/kcj.2018.0296
Results We performed a systemic meta-analysis of 17 studies (12 randomized controlled studies and 5 non-randomized registries) which compared clinical outcomes of 9,101 patients who underwent CABG with or without preoperative aspirin administration.
Results We performed a systemic meta-analysis of 17 studies (12 randomized controlled studies and 5 non-randomized registries) which compared clinical outcomes of 9,101 patients who underwent CABG with or without preoperative aspirin administration.
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10.1371/journal.pone.0221067
Our quantitative synthesis included 12 randomized control trials and 2 non-randomized control trials, with the follow-up period ranging from 4 to 52 weeks.
Our quantitative synthesis included 12 randomized control trials and 2 non-randomized control trials, with the follow-up period ranging from 4 to 52 weeks.
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10.1089/end.2019.0520
RESULTS
Of 3338 records, 26 were screened as full-text and 12 randomized controlled trials were included totaling 1352 patients.
RESULTS
Of 3338 records, 26 were screened as full-text and 12 randomized controlled trials were included totaling 1352 patients.
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10.4103/1673-5374.249228
Results: After screening 1717 citations, 12 randomized controlled trials were included.
Results: After screening 1717 citations, 12 randomized controlled trials were included.
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10.1177/2473011419s00030
Results: Twenty-four patients (24 lower extremities) were enrolled in the study and 12 randomized to each group.
Results: Twenty-four patients (24 lower extremities) were enrolled in the study and 12 randomized to each group.
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10.1161/JAHA.119.012184
After screening 10 644 articles, 12 randomized controlled trials including 14 906 patients were included in the final analyses.
After screening 10 644 articles, 12 randomized controlled trials including 14 906 patients were included in the final analyses.
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10.1007/s00484-019-01780-4
We screened the PubMed, EMBASE, Cochrane Library, China Science and Technology Journal, China National Knowledge Infrastructure, WANFANG, and China Biology Medicine disc databases and selected 12 randomized controlled trials involving a total of 1122 participants.
We screened the PubMed, EMBASE, Cochrane Library, China Science and Technology Journal, China National Knowledge Infrastructure, WANFANG, and China Biology Medicine disc databases and selected 12 randomized controlled trials involving a total of 1122 participants.
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10.1097/JU.0000000000000399
RESULTS
Data from 12 randomized-controlled trials on 1,549 patients were included in the final intraurethral lidocaine meta-analysis.
RESULTS
Data from 12 randomized-controlled trials on 1,549 patients were included in the final intraurethral lidocaine meta-analysis.
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10.2174/1871530319666191107110420
RESULTS
12 randomized controlled trials with 994 participants were included.
RESULTS
12 randomized controlled trials with 994 participants were included.
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10.3851/IMP3299
From 2006 to 2011, 12 randomized sites provided either routine VL monitoring (intervention) or discretionary (control) after ART initiation.
From 2006 to 2011, 12 randomized sites provided either routine VL monitoring (intervention) or discretionary (control) after ART initiation.
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10.1155/2019/7918631
Results Eventually, a total of 12 randomized controlled trials were included in this systematic review.
Results Eventually, a total of 12 randomized controlled trials were included in this systematic review.
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10.1016/j.arthro.2019.06.033
RESULTS
A final group of 12 randomized controlled trials were included that enrolled a total of 659 patients with knee cartilage lesions: 332 patients had received ACI and 327 patients had undergone MF.
RESULTS
A final group of 12 randomized controlled trials were included that enrolled a total of 659 patients with knee cartilage lesions: 332 patients had received ACI and 327 patients had undergone MF.
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10.1245/s10434-019-07491-9
This differs from Western methodology, which is rooted in the landmark 2012 randomized ChemoRadiotherapy for Oesophageal cancer followed by Surgery Study (CROSS) trial, which demonstrated a clear difference in median overall survival of 49.
This differs from Western methodology, which is rooted in the landmark 2012 randomized ChemoRadiotherapy for Oesophageal cancer followed by Surgery Study (CROSS) trial, which demonstrated a clear difference in median overall survival of 49.
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10.13188/2377-9292.1000021
Methods: Using a defined selection criterion, a literature search identified 12 Randomized Clinical Trials (RCTs) involving 7,095 patients where CPIs have been used in the first-line setting.
Methods: Using a defined selection criterion, a literature search identified 12 Randomized Clinical Trials (RCTs) involving 7,095 patients where CPIs have been used in the first-line setting.
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