The CONSORT statement: revised recommendations for improving the quality of reports of parallel-group randomised trials
To comprehend the results of a randomised controlled trial (RCT), readers must understand
its design, conduct, analysis, and interpretation. That goal can be achieved only through …
its design, conduct, analysis, and interpretation. That goal can be achieved only through …
The CONSORT Statement: revised recommendations for improving the quality of reports of parallel-group randomized trials 2001
To comprehend the results of a randomized controlled trial (RCT), readers must understand
its design, conduct, analysis, and interpretation. That goal can be achieved only through …
its design, conduct, analysis, and interpretation. That goal can be achieved only through …
CONSORT 2010 statement: updated guidelines for reporting parallel group randomised trials
Randomised controlled trials, when appropriately designed, conducted and reported,
represent the gold standard in evaluating healthcare interventions. However, randomised …
represent the gold standard in evaluating healthcare interventions. However, randomised …
Reporting of multi-arm parallel-group randomized trials: extension of the CONSORT 2010 statement
Importance The quality of reporting of randomized clinical trials is suboptimal. In an era in
which the need for greater research transparency is paramount, inadequate reporting …
which the need for greater research transparency is paramount, inadequate reporting …
The CONSORT statement: revised recommendations for improving the quality of reports of parallel-group randomised trials
To comprehend the results of a randomised controlled trial (RCT), readers must understand
its design, conduct, analysis, and interpretation. That goal can be achieved only through …
its design, conduct, analysis, and interpretation. That goal can be achieved only through …
The quality of randomized trial reporting in leading medical journals since the revised CONSORT statement
If randomized controlled trials (RCTs) are to fulfill their potential to allow health care
providers to make informed inferences about the validity of the trials upon which they base …
providers to make informed inferences about the validity of the trials upon which they base …
Selective reporting in clinical trials: analysis of trial protocols accepted by The Lancet
Selective reporting in clinical trials occurs when outcome data are collected but not reported,
and when investigators do many analyses but report only the most favourable. It can distort …
and when investigators do many analyses but report only the most favourable. It can distort …
CONSORT 2010 explanation and elaboration: updated guidelines for reporting parallel group randomised trials
Overwhelming evidence shows the quality of reporting of randomised controlled trials
(RCTs) is not optimal. Without transparent reporting, readers cannot judge the reliability and …
(RCTs) is not optimal. Without transparent reporting, readers cannot judge the reliability and …
Reducing waste from incomplete or unusable reports of biomedical research
Research publication can both communicate and miscommunicate. Unless research is
adequately reported, the time and resources invested in the conduct of research is wasted …
adequately reported, the time and resources invested in the conduct of research is wasted …
Improving the reporting of randomised trials: the CONSORT Statement and beyond
An extensive and growing number of reviews of the published literature demonstrate that
health research publications have frequent deficiencies. Of particular concern are poor …
health research publications have frequent deficiencies. Of particular concern are poor …