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Prevalence, characteristics, and publication of discontinued randomized trials.

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TLDR
Great efforts are needed to ensure the reporting of trial discontinuation to research ethics committees and the publication of results of discontinued trials, with poor recruitment being the most frequently reported reason.
Abstract
Importance The discontinuation of randomized clinical trials (RCTs) raises ethical concerns and often wastes scarce research resources. The epidemiology of discontinued RCTs, however, remains unclear. Objectives To determine the prevalence, characteristics, and publication history of discontinued RCTs and to investigate factors associated with RCT discontinuation due to poor recruitment and with nonpublication. Design and Setting Retrospective cohort of RCTs based on archived protocols approved by 6 research ethics committees in Switzerland, Germany, and Canada between 2000 and 2003. We recorded trial characteristics and planned recruitment from included protocols. Last follow-up of RCTs was April 27, 2013. Main Outcomes and Measures Completion status, reported reasons for discontinuation, and publication status of RCTs as determined by correspondence with the research ethics committees, literature searches, and investigator surveys. Results After a median follow-up of 11.6 years (range, 8.8-12.6 years), 253 of 1017 included RCTs were discontinued (24.9% [95% CI, 22.3%-27.6%]). Only 96 of 253 discontinuations (37.9% [95% CI, 32.0%-44.3%]) were reported to ethics committees. The most frequent reason for discontinuation was poor recruitment (101/1017; 9.9% [95% CI, 8.2%-12.0%]). In multivariable analysis, industry sponsorship vs investigator sponsorship (8.4% vs 26.5%; odds ratio [OR], 0.25 [95% CI, 0.15-0.43]; P P  = .04) were associated with lower rates of discontinuation due to poor recruitment. Discontinued trials were more likely to remain unpublished than completed trials (55.1% vs 33.6%; OR, 3.19 [95% CI, 2.29-4.43]; P Conclusions and Relevance In this sample of trials based on RCT protocols from 6 research ethics committees, discontinuation was common, with poor recruitment being the most frequently reported reason. Greater efforts are needed to ensure the reporting of trial discontinuation to research ethics committees and the publication of results of discontinued trials.

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Terminated Trials in the ClinicalTrials.gov Results Database: Evaluation of Availability of Primary Outcome Data and Reasons for Termination.

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References
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Clinical Trial Registration A Statement From the International Committee of Medical Journal Editors

TL;DR: The Editors and the Scientific Publishing Committee of the American Heart Association journals support the principles enunciated in the editorial “Clinical Trial Registration: A Statement from the International Committee of Medical Journal Editors.”
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What influences recruitment to randomised controlled trials? A review of trials funded by two UK funding agencies.

TL;DR: Factors that may have been associated with good and poor recruitment in a cohort of multicentre trials funded by two public bodies, identified from the administrative databases held by the two funding bodies, are explored.
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Publication bias: evidence of delayed publication in a cohort study of clinical research projects

TL;DR: The study results support the need for prospective registration of clinical research projects to avoid publication bias and also support restricting the selection of trials to those started before a common date in undertaking systematic reviews.
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