CONSORT 2010 explanation and elaboration: updated guidelines for reporting parallel group randomised trials

D Moher, S Hopewell, KF Schulz, V Montori… - Bmj, 2010 - bmj.com
Overwhelming evidence shows the quality of reporting of randomised controlled trials
(RCTs) is not optimal. Without transparent reporting, readers cannot judge the reliability and …

CONSORT 2010 statement: updated guidelines for reporting parallel group randomised trials

KF Schulz, DG Altman, D Moher - Journal of Pharmacology …, 2010 - journals.sagepub.com
Randomised controlled trials, when appropriately designed, conducted and reported,
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 …

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 …

CONSORT 2010 statement: extension to randomised crossover trials

K Dwan, T Li, DG Altman, D Elbourne - bmj, 2019 - bmj.com
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 …

CONSORT 2010 statement: extension to randomised pilot and feasibility trials

SM Eldridge, CL Chan, MJ Campbell, CM Bond… - bmj, 2016 - bmj.com
The Consolidated Standards of Reporting Trials (CONSORT) statement is a guideline
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 …

Frequency and reasons for outcome reporting bias in clinical trials: interviews with trialists

RMD Smyth, JJ Kirkham, A Jacoby, DG Altman… - Bmj, 2011 - bmj.com
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 …

Improving the reporting of pragmatic trials: an extension of the CONSORT statement

M Zwarenstein, S Treweek, JJ Gagnier, DG Altman… - Bmj, 2008 - bmj.com
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 …

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 …