Reporting of surrogate endpoints in randomised controlled trial reports (CONSORT-Surrogate): extension checklist with explanation and elaboration-Reference-Cited by-同舟云学术

Reporting of surrogate endpoints in randomised controlled trial reports (CONSORT-Surrogate): extension checklist with explanation and elaboration

Published:2024-07-09 Issue: Volume: Page:e078524
ISSN:1756-1833
Container-title:BMJ
language:en
Short-container-title:BMJ

Author:

Manyara Anthony Muchai,Davies Philippa,Stewart Derek,Weir Christopher J,Young Amber E,Blazeby Jane,Butcher Nancy J,Bujkiewicz Sylwia,Chan An-Wen,Dawoud Dalia,Offringa Martin,Ouwens Mario,Hróbjartssson Asbjørn,Amstutz Alain,Bertolaccini Luca,Bruno Vito Domenico,Devane Declan,Faria Christina D C M,Gilbert Peter B,Harris Ray,Lassere Marissa,Marinelli Lucio,Markham Sarah,Powers John H,Rezaei Yousef,Richert Laura,Schwendicke Falk,Tereshchenko Larisa G,Thoma Achilles,Turan Alparslan,Worrall Andrew,Christensen Robin,Collins Gary S,Ross Joseph S,Taylor Rod S,Ciani Oriana^ORCID

Funder

Medical Research Council

Publisher

BMJ

Reference112 articles.

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2. Avoidable waste in the production and reporting of research evidence

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4. CONSORT 2010 Explanation and Elaboration: updated guidelines for reporting parallel group randomised trials

5. Does use of the CONSORT Statement impact the completeness of reporting of randomised controlled trials published in medical journals? A Cochrane reviewa

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2. Surrogate End Points in Trials—SPIRIT and CONSORT Extensions;JAMA;2024-08-05

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4. Transparent and complete reporting of surrogate endpoints in trials: the SPIRIT-Surrogate and CONSORT-Surrogate extensions;The Lancet;2024-07