Article

Guideline on the design and conduct of cystic fibrosis clinical trials: the European Cystic Fibrosis Society-Clinical Trials Network (ECFS-CTN).

Department of Pediatrics, University Hospital of Leuven, Leuven, Belgium.
Journal of cystic fibrosis: official journal of the European Cystic Fibrosis Society (impact factor: 3.19). 06/2011; 10 Suppl 2:S67-74. DOI:10.1016/S1569-1993(11)60010-6 pp.S67-74
Source: PubMed

ABSTRACT We describe the rationale for disease specific research networks in general as well as the aims and function of the European Cystic Fibrosis Society-Clinical Trials Network (ECFS-CTN) specifically. The ECFS-CTN was founded in 2009 with the aim of improving the quality and quantity of clinical research in the area of cystic fibrosis (CF) in Europe. A network of 18 clinical trial sites in 8 European countries was established according to uniform state-of-the-art quality criteria. To support the ECFS-CTN in the acquisition, planning and conduct of clinical trials, the network is equipped with a coordinating centre, steering and executive committees, and committees for protocol review, standardization, training and networking as well as a data safety monitoring board. A strong partnership with European CF patient parent organizations aims to increase awareness of the need for efficient clinical research and the participation of patients in clinical trials.

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Keywords

18 clinical trial sites
 
8 European countries
 
committees
 
coordinating centre
 
cystic fibrosis
 
data safety monitoring board
 
Europe
 
European CF patient parent organizations
 
European Cystic Fibrosis Society-Clinical Trials Network
 
executive committees
 
increase awareness
 
patients
 
protocol review
 
uniform state-of-the-art quality criteria