Prospective registration and reporting of trial number in randomised clinical trials: global cross sectional study of the adoption of ICMJE and Declaration of Helsinki …

M Al-Durra, RP Nolan, E Seto, JA Cafazzo - bmj, 2020 - bmj.com
Objectives To evaluate the compliance with prospective registration and inclusion of the trial
registration number (TRN) in published randomised controlled trials (RCTs), and to analyse …

[引用][C] Registry randomized controlled trials: the future of surgical trials?

Y Arafat, MY Wei, B Karanatsios, S Mendis… - ANZ Journal of …, 2023 - Wiley Online Library
Randomized controlled trials (RCTs) provide the highest level of evidence in clinical
research and are the foundation of evidencebased medicine. 1 However, ongoing …

[引用][C] A review of prospective trial registration in the Journal of Advanced Nursing in 2018

R Gray, E Brown, G Gray - Journal of Advanced Nursing, 2019 - Wiley Online Library
1 BACKGROUND Registration creates a public record of planned clinical trials and is
perhaps that most important weapon in ensuring unbiased reporting of clinical research. It is …

The ideal reporting guidelines: a Delphi consensus statement stage specific recommendations for reporting the evaluation of surgical innovation

NA Bilbro, A Hirst, A Paez, B Vasey, M Pufulete… - Annals of …, 2021 - journals.lww.com
Objective: The aim of this study was to define reporting standards for IDEAL format studies.
Background: The IDEAL Framework and Recommendations establish an integrated …

Issues in the registration of clinical trials

DA Zarin, NC Ide, T Tse, WR Harlan, JC West… - Jama, 2007 - jamanetwork.com
Public concerns about the perils associated with incomplete or delayed reporting of results
from clinical trials has heightened interest in trial registries and results databases. Here we …

From registration to publication: A study on Dutch academic randomized controlled trials

J Huiskens, BRJ Kool, JM Bakker… - Research synthesis …, 2020 - Wiley Online Library
Introduction Registration of clinical trials has been initiated in order to assess adherence of
the reported results to the original trial protocol. This study aimed to investigate the …

Can Orthopaedics become the Gold Standard for Reproducibility? A Roadmap to Success

IA Fladie, S Evans, J Checketts, D Tritz, B Norris… - bioRxiv, 2019 - biorxiv.org
Background Scientific research is replete with poor accessibility to data, materials, and
protocol, which limits the reproducibility of a study. Transparency with regard to materials …

[HTML][HTML] Update on trials registration: clinical trial registration: looking back and moving ahead

C Laine, R Horton, CD DeAngelis… - … of Medical Journal …, 2007 - icmje.acponline.org
In 2005, the International Committee of Medical Journal Editors (ICMJE) initiated a policy
requiring investigators to deposit information about trial design into an accepted clinical …

[HTML][HTML] Identifying research waste from surgical research: a protocol for assessing compliance with the IDEAL framework and recommendations

J Yu, F Shan, A Hirst, P McCulloch, Y Li… - … surgery, interventions, & …, 2021 - ncbi.nlm.nih.gov
Methods We will search for potential studies published in English and between 1 January
2018 and 31 December 2018 via PubMed. Teams of paired reviewers will screen titles …

Non-existent ClinicalTrials. gov identifiers in abstracts indexed by PubMed

BG Carlisle - medRxiv, 2020 - medrxiv.org
Prospective registration plays an important role in ensuring the transparency and reliability
of clinical trials. Preregistration of clinical trials has been required by the ICMJE since 2005 …