Multicenter Evaluation of Infant Lung Function Tests as Cystic Fibrosis Clinical Trial Endpoints

Rationale: The conducting of clinical trials in infants with cystic fibrosis (CF) has been hindered by lack of sensitive outcome measures. Objectives: To evaluate safety, feasibility, and ability to detect abnormalities in lung function of serial pulmonary function tests (PFTs) in infants with CF. M...

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Bibliographische Detailangaben
Hauptverfasser: Davis, Stephanie D., Rosenfeld, Margaret, Kerby, Gwendolyn S., Brumback, Lyndia, Kloster, Margaret H., Acton, James D., Colin, Andrew A., Conrad, Carol K., Hart, Meeghan A., Hiatt, Peter W., Mogayzel, Peter J., Johnson, Robin C., Wilcox, Stephanie L., Castile, Robert G.
Format: Artigo
Sprache:Inglês
Veröffentlicht: American Thoracic Society 2010
Schlagworte:
D. Cystic Fibrosis
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3159081/
https://ncbi.nlm.nih.gov/pubmed/20622043
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.200908-1236OC
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