Paper I: Heterogeneous use of registry data for participant identification and primary outcome ascertainment is found in registry-based randomized controlled trials: A scoping review-Reference-Cited by-同舟云学术

Paper I: Heterogeneous use of registry data for participant identification and primary outcome ascertainment is found in registry-based randomized controlled trials: A scoping review

Published:2023-07 Issue: Volume:159 Page:289-299
ISSN:0895-4356
Container-title:Journal of Clinical Epidemiology
language:en
Short-container-title:Journal of Clinical Epidemiology

Author:

Baba Ami^ORCID,Tay Joanne,Sammy Adrian,Douglas William A.,Goren Katherine,Krause Karolin R.,Howie Alison H.,Little Julian,Oskoui Maryam,Taljaard Monica,Thombs Brett D.,Potter Beth K.,Butcher Nancy J.,Offringa Martin^ORCID

Publisher

Elsevier BV

Subject

Epidemiology

Reference35 articles.

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3. Protocol for the development of a CONSORT extension for RCTs using cohorts and routinely collected health data;Kwakkenbos;Res Integrity Peer Rev,2018

4. Reporting transparency and completeness in Trials: paper 2 - reporting of randomised trials using registries was often inadequate and hindered the interpretation of results;McCord;J Clin Epidemiol,2022

5. Rare disease registries: potential applications towards impact on development of new drug treatments;Jansen-van der Weide;Orphanet J Rare Dis,2018

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