Literature DB >> 29638145

Prevalence and reporting of recruitment, randomisation and treatment errors in clinical trials: A systematic review.

Lisa N Yelland1,2, Brennan C Kahan3, Elsa Dent4, Katherine J Lee5,6, Merryn Voysey7, Andrew B Forbes8, Jonathan A Cook9,10.   

Abstract

Background/aims In clinical trials, it is not unusual for errors to occur during the process of recruiting, randomising and providing treatment to participants. For example, an ineligible participant may inadvertently be randomised, a participant may be randomised in the incorrect stratum, a participant may be randomised multiple times when only a single randomisation is permitted or the incorrect treatment may inadvertently be issued to a participant at randomisation. Such errors have the potential to introduce bias into treatment effect estimates and affect the validity of the trial, yet there is little motivation for researchers to report these errors and it is unclear how often they occur. The aim of this study is to assess the prevalence of recruitment, randomisation and treatment errors and review current approaches for reporting these errors in trials published in leading medical journals. Methods We conducted a systematic review of individually randomised, phase III, randomised controlled trials published in New England Journal of Medicine, Lancet, Journal of the American Medical Association, Annals of Internal Medicine and British Medical Journal from January to March 2015. The number and type of recruitment, randomisation and treatment errors that were reported and how they were handled were recorded. The corresponding authors were contacted for a random sample of trials included in the review and asked to provide details on unreported errors that occurred during their trial. Results We identified 241 potentially eligible articles, of which 82 met the inclusion criteria and were included in the review. These trials involved a median of 24 centres and 650 participants, and 87% involved two treatment arms. Recruitment, randomisation or treatment errors were reported in 32 in 82 trials (39%) that had a median of eight errors. The most commonly reported error was ineligible participants inadvertently being randomised. No mention of recruitment, randomisation or treatment errors was found in the remaining 50 of 82 trials (61%). Based on responses from 9 of the 15 corresponding authors who were contacted regarding recruitment, randomisation and treatment errors, between 1% and 100% of the errors that occurred in their trials were reported in the trial publications. Conclusion Recruitment, randomisation and treatment errors are common in individually randomised, phase III trials published in leading medical journals, but reporting practices are inadequate and reporting standards are needed. We recommend researchers report all such errors that occurred during the trial and describe how they were handled in trial publications to improve transparency in reporting of clinical trials.

Entities:  

Keywords:  Randomisation error; ineligible participant; randomised controlled trial; reporting recommendations

Mesh:

Year:  2018        PMID: 29638145     DOI: 10.1177/1740774518761627

Source DB:  PubMed          Journal:  Clin Trials        ISSN: 1740-7745            Impact factor:   2.486


  5 in total

1.  Trial and error: challenges conducting pragmatic trials in general practice.

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Journal:  Br J Gen Pract       Date:  2022-01-27       Impact factor: 5.386

2.  Sample size calculation in multi-centre clinical trials.

Authors:  Markus Harden; Tim Friede
Journal:  BMC Med Res Methodol       Date:  2018-11-29       Impact factor: 4.615

3.  A Network Analysis of Multiple Myeloma Related Gene Signatures.

Authors:  Yu Liu; Haocheng Yu; Seungyeul Yoo; Eunjee Lee; Alessandro Laganà; Samir Parekh; Eric E Schadt; Li Wang; Jun Zhu
Journal:  Cancers (Basel)       Date:  2019-09-27       Impact factor: 6.639

4.  Assessing the potential for prevention or earlier detection of on-site monitoring findings from randomised controlled trials: Further analyses of findings from the prospective TEMPER triggered monitoring study.

Authors:  William J Cragg; Caroline Hurley; Victoria Yorke-Edwards; Sally P Stenning
Journal:  Clin Trials       Date:  2020-11-24       Impact factor: 2.486

Review 5.  Adherence to participant flow diagrams in trials on postoperative pain management after total hip and knee arthroplasty: a methodological review.

Authors:  Thea Nørgaard Rønsbo; Jens Laigaard; Casper Pedersen; Ole Mathiesen; Anders Peder Højer Karlsen
Journal:  Trials       Date:  2021-04-14       Impact factor: 2.279

  5 in total

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