Talk:Clinical trial registration

Latest comment: 4 years ago by Klbrain in topic Merge into preregistration

Improve explaination World Health Organisation’s International Clinical Trials Registry Platform

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On reading this it strikes me that the WHO plaform is the one most others feed into - so this should be made clearer in the article? Or have I misunderstood? Jack Nunn 04:13, 26 June 2018 (UTC) — Preceding unsigned comment added by Jacknunn (talkcontribs)

Merge from Trial_registration

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The Clinical_trials_registry article currently covers both the concept of trial registration, as well as the registries themselves. I'd therefore suggest merging and redirecting Trial_registration to it. T.Shafee(Evo&Evo)talk 02:02, 14 March 2019 (UTC)Reply

Merge into preregistration

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Based on my understanding of the two topics, this seem appropriate. But I'm not an expert, so would welcome more input here. Scientific29 (talk) 15:09, 5 January 2020 (UTC)Reply

The discussion of this topic is more extensive on the other page ... Talk:Preregistration#Merge clinical trial registration into this article. Klbrain (talk) 16:50, 19 April 2020 (UTC)Reply

Add 2017 guide

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File:Clinical Trial Transparency 2017.pdf
Clincal Trial Transparency, a 2017 policy guide, argues for registration

I added this guide to the top of the article. It is free media, seems relevant, and has expert backing of Cochrane (organisation) and Transparency International. Blue Rasberry (talk) 21:32, 13 January 2020 (UTC)Reply

Narrative of history

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This is United States history, but it also is a narrative of what to expect of a registry.

  • Todd, JL; White, KR; Chiswell, K; Tasneem, A; Palmer, SM (October 2013). "Using ClinicalTrials.gov to understand the state of clinical research in pulmonary, critical care, and sleep medicine". Annals of the American Thoracic Society. 10 (5): 411–7. doi:10.1513/AnnalsATS.201305-111OC. PMID 23987571.

I always like seeing anyone publish history of policy or why things happen the way they do.

November 21, 1997 government must create a clinical trials registry
February 29, 2000 ClinicalTrials.gov comes online
September 16, 2004 ICMJE recommendations mandates that it research journals should exclude outcomes from non-registered trials
September 27, 2007 Food and Drug Administration Amendments Act of 2007 section 801 mandates registration and penalty for noncompliance
September 27, 2008 reporting results is mandatory
September 27, 2009 reporting adverse events is mandatory

Blue Rasberry (talk) 15:37, 4 February 2020 (UTC)Reply