Literature DB >> 19399943

Centralized national ethical review of clinical trials in Croatia.

Dinko Vitezić1, Maja Lovrek, Sinisa Tomić.   

Abstract

AIM: To present the Croatian system of ethical review of clinical trials and assessment outcomes of the applications reviewed by the Croatian Central Ethics Committee.
METHODS: Clinical trial applications reviewed by the Croatian Central Ethics Committee, which has the legal mandate to review clinical trials of medicinal products and medical devices, were retrospectively analyzed from May 2004 to the end of 2008 according to the number, research area, and type of opinion issued. Applications from 2008 were analyzed separately according to the study phase, participants (adult trials vs pediatric trials), and sponsor (commercial trials vs academic trials). Data were analyzed by descriptive statistics.
RESULTS: Since its establishment in 2004, the Croatian Central Ethics Committee has reviewed 407 trials. The greatest number of clinical trials was in the field of oncology (n = 69), mental and behavioral disorders (n = 52), and endocrine, nutritional, and metabolic diseases (n = 50). In the initial assessment of clinical trials, 60% applications received a conditionally positive opinion. In 28% of applications, the opinion had to be postponed because additional documentation or explanations were required. In 2008, the Croatian Central Ethics Committee reviewed 99 trials, most of which were phase III trials (n = 57). Five clinical trials included pediatric population and 3 were academic clinical trials.
CONCLUSION: The model of centralized clinical trial review seems to be appropriate for the current number of clinical trials conducted in Croatia. The efficient and standardized review process of clinical trials by the Central Ethics Committee may positively affect the increasing number of clinical trials conducted in Croatia. Future development includes the transparency of the clinical trials through a publically available database and establishing the basis for conducting academic clinical trials.

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Year:  2009        PMID: 19399943      PMCID: PMC2681057          DOI: 10.3325/cmj.2009.50.111

Source DB:  PubMed          Journal:  Croat Med J        ISSN: 0353-9504            Impact factor:   1.351


  9 in total

1.  Performance of research ethics committees in Spain. A prospective study of 100 applications for clinical trial protocols on medicines.

Authors:  R Dal-Ré; J Espada; R Ortega
Journal:  J Med Ethics       Date:  1999-06       Impact factor: 2.903

2.  Who's afraid of the European clinical trials Directive?

Authors: 
Journal:  Lancet       Date:  2003-06-28       Impact factor: 79.321

3.  Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the member states relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use.

Authors: 
Journal:  Med Etika Bioet       Date:  2002 Spring-Summer

4.  Effect of European Clinical Trials Directive on academic drug trials in Denmark: retrospective study of applications to the Danish Medicines Agency 1993-2006.

Authors:  Louise Berendt; Cecilia Håkansson; Karin Friis Bach; Kim Dalhoff; Per Buch Andreasen; Lene Grejs Petersen; Elin Andersen; Henrik Enghusen Poulsen
Journal:  BMJ       Date:  2007-12-06

5.  Cross district comparison of applications to research ethics committees.

Authors:  P Garfield
Journal:  BMJ       Date:  1995-09-09

6.  Delays and diversity in the practice of local research ethics committees.

Authors:  A H Ahmed; K G Nicholson
Journal:  J Med Ethics       Date:  1996-10       Impact factor: 2.903

7.  Research ethics committees at work: the experience of one multi-location study.

Authors:  A E While
Journal:  J Med Ethics       Date:  1996-12       Impact factor: 2.903

8.  Variation in institutional review board responses to a standard, observational, pediatric research protocol.

Authors:  Jonathan Mansbach; Uchechi Acholonu; Sunday Clark; Carlos A Camargo
Journal:  Acad Emerg Med       Date:  2007-02-20       Impact factor: 3.451

9.  Variation in standards of research compensation and child assent practices: a comparison of 69 institutional review board-approved informed permission and assent forms for 3 multicenter pediatric clinical trials.

Authors:  Michael B Kimberly; K Sarah Hoehn; Chris Feudtner; Robert M Nelson; Mark Schreiner
Journal:  Pediatrics       Date:  2006-05       Impact factor: 7.124

  9 in total
  1 in total

1.  Croatian National Centre for Biobanking--a new perspective in biobanks governance?

Authors:  Ana Borovečki; Luciana Caenazzo; Davor Ježek; Monika Karija-Vlahović; Branka Golubić
Journal:  Croat Med J       Date:  2014-08-28       Impact factor: 1.351

  1 in total

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