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 …
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 …
The new CONSORT statement
G Antes - Bmj, 2010 - bmj.com
Full and transparent reporting of results of clinical trials is essential for assessing the quality
of healthcare interventions. Inadequate reporting of trials is common, and it impedes the use …
of healthcare interventions. Inadequate reporting of trials is common, and it impedes the use …
Better reporting of randomised controlled trials: the CONSORT statement
DG Altman - Bmj, 1996 - bmj.com
Randomised controlled trials are the best way to compare the effectiveness of different
interventions. Only randomised trials allow valid inferences of cause and effect. Only …
interventions. Only randomised trials allow valid inferences of cause and effect. Only …
CONSORT 2010 statement: extension to randomised crossover trials
Evidence shows the quality of reporting of randomised controlled trials is not optimal. The
lack of transparent reporting impedes readers from judging the reliability and validity of trial …
lack of transparent reporting impedes readers from judging the reliability and validity of trial …
CONSORT 2010 statement: extension to randomised pilot and feasibility trials
The Consolidated Standards of Reporting Trials (CONSORT) statement is a guideline
designed to improve the transparency and quality of the reporting of randomised controlled …
designed to improve the transparency and quality of the reporting of randomised controlled …
CONSORT 2010 statement: extension checklist for reporting within person randomised trials
N Pandis, B Chung, RW Scherer, D Elbourne… - Bmj, 2017 - bmj.com
Evidence shows that the quality of reporting of randomised controlled trials (RCTs) is not
optimal. The lack of transparent reporting impedes readers from judging the reliability and …
optimal. The lack of transparent reporting impedes readers from judging the reliability and …
Frequency and reasons for outcome reporting bias in clinical trials: interviews with trialists
Objectives To provide information on the frequency and reasons for outcome reporting bias
in clinical trials. Design Trial protocols were compared with subsequent publication (s) to …
in clinical trials. Design Trial protocols were compared with subsequent publication (s) to …
Improving the reporting of pragmatic trials: an extension of the CONSORT statement
Background The CONSORT statement is intended to improve reporting of randomised
controlled trials and focuses on minimising the risk of bias (internal validity). The applicability …
controlled trials and focuses on minimising the risk of bias (internal validity). The applicability …
CONSORT extension for the reporting of randomised controlled trials conducted using cohorts and routinely collected data (CONSORT-ROUTINE): checklist with …
L Kwakkenbos, M Imran, SJ McCall, KA McCord… - bmj, 2021 - bmj.com
Randomised controlled trials are increasingly conducted as embedded, nested, or using
cohorts or routinely collected data, including registries, electronic health records, and …
cohorts or routinely collected data, including registries, electronic health records, and …