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

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

Published:2024-07-09 Issue: Volume: Page:e078525
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

Reference115 articles.

1. CONSORT Harms 2022 statement, explanation, and elaboration: updated guideline for the reporting of harms in randomised trials

2. SPIRIT 2013 explanation and elaboration: guidance for protocols of clinical trials

3. World Medical Association Declaration of Helsinki

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

5. Reducing waste from incomplete or unusable reports of biomedical research

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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