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
- 3 May 2023
- journal article
- review article
- Published by Elsevier in Journal of Clinical Epidemiology
- Vol. 159, 289-299
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Protocol for the development of a CONSORT extension for RCTs using cohorts and routinely collected health dataResearch Integrity and Peer Review, 2018
- Rare disease registries: potential applications towards impact on development of new drug treatmentsOrphanet Journal of Rare Diseases, 2018
- Association of Trial Registration With Reporting of Primary Outcomes in Protocols and PublicationsJAMA, 2017
- Bivalirudin versus Heparin Monotherapy in Myocardial InfarctionNew England Journal of Medicine, 2017
- Registry-based randomized controlled trials- what are the advantages, challenges, and areas for future research?Journal of Clinical Epidemiology, 2016
- A Core Outcome Set for Children With Feeding Tubes and Neurologic Impairment: A Systematic ReviewPediatrics, 2016
- Outcome reporting in randomised controlled trials and meta-analyses of appendicitis treatments in children: a systematic reviewTrials, 2015
- Registry-based randomized clinical trials—a new clinical trial paradigmNature Reviews Cardiology, 2015
- The quality of reports of randomised trials in 2000 and 2006: comparative study of articles indexed in PubMedBMJ, 2010
- Research electronic data capture (REDCap)—A metadata-driven methodology and workflow process for providing translational research informatics supportJournal of Biomedical Informatics, 2009