Literature DB >> 17957593

[Evaluation of clinical trials following an approval from a research ethics committee].

S Menzel1, B Uebing, P Hucklenbroich, O Schober.   

Abstract

BACKGROUND AND
OBJECTIVE: According to the Medical Association's professional code of conduct a consultation of the responsible ethics committee has to be undertaken prior to biomedical research. Up to date there has been no systematic analysis of published results after an approval from the research ethics committee of the Medical Association Westfalen-Lippe. A measure for the importance are publications of concluded trials. This work presents a comprehensive collection and evaluation of clinical trials that were approved in 1996.
METHODS: Clinical trials that were approved by the ethics committee in the year 1996 were analysed concerning their publication parameters, if results have been reported to the ethics committee, the design of the study and their funding. Publications were found by database mining in the Internet sources "Pubmed" and "ISI Web of Knowledge".
RESULTS: 70 % out of the 99 approved clinical trials were published as specified in the initial proposal, whereas in 2 % only aspects of the proposal were published. In 21 % of the cases only publications in closely related subjects could be identified. 7 % however remained unpublished. Of these studies 63 % were designed as mono centre study and 37 % as multi centre studies. The time from approval of the study until publication was 46 months (median value). Furthermore the analysis revealed, that 45 % of the studies were funded by industry.
CONCLUSION: This work represents an unprecedented and detailed analysis of the clinical studies approved by a German ethics committee. In the course of this work a comprehensive catalogue with criteria to facilitate a collection and tracking mechanism was established. This should enable the ethics committee to comply with their new duties. A great amount of the clinical trials were presented in publications to the scientific community.

Mesh:

Year:  2007        PMID: 17957593     DOI: 10.1055/s-2007-991648

Source DB:  PubMed          Journal:  Dtsch Med Wochenschr        ISSN: 0012-0472            Impact factor:   0.628


  6 in total

Review 1.  Publication bias in clinical trials due to statistical significance or direction of trial results.

Authors:  Sally Hopewell; Kirsty Loudon; Mike J Clarke; Andrew D Oxman; Kay Dickersin
Journal:  Cochrane Database Syst Rev       Date:  2009-01-21

2.  [The urological trial registry of the German Society of Urology].

Authors:  F Kunath; C Becker; S Jena; G Antes; B Wullich
Journal:  Urologe A       Date:  2011-04       Impact factor: 0.639

3.  Comparison of protocols and registry entries to published reports for randomised controlled trials.

Authors:  Kerry Dwan; Douglas G Altman; Lynne Cresswell; Michaela Blundell; Carrol L Gamble; Paula R Williamson
Journal:  Cochrane Database Syst Rev       Date:  2011-01-19

4.  Extent of non-publication in cohorts of studies approved by research ethics committees or included in trial registries.

Authors:  Christine Schmucker; Lisa K Schell; Susan Portalupi; Patrick Oeller; Laura Cabrera; Dirk Bassler; Guido Schwarzer; Roberta W Scherer; Gerd Antes; Erik von Elm; Joerg J Meerpohl
Journal:  PLoS One       Date:  2014-12-23       Impact factor: 3.240

Review 5.  Systematic review of the empirical evidence of study publication bias and outcome reporting bias.

Authors:  Kerry Dwan; Douglas G Altman; Juan A Arnaiz; Jill Bloom; An-Wen Chan; Eugenia Cronin; Evelyne Decullier; Philippa J Easterbrook; Erik Von Elm; Carrol Gamble; Davina Ghersi; John P A Ioannidis; John Simes; Paula R Williamson
Journal:  PLoS One       Date:  2008-08-28       Impact factor: 3.240

Review 6.  Systematic review of the empirical evidence of study publication bias and outcome reporting bias - an updated review.

Authors:  Kerry Dwan; Carrol Gamble; Paula R Williamson; Jamie J Kirkham
Journal:  PLoS One       Date:  2013-07-05       Impact factor: 3.240

  6 in total

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