Randomized, single blind, controlled trial of inhaled glutathione vs placebo in patients with cystic fibrosis C. Calabrese, A. Tosco, P. Abete, V. Carnovale, C. Basile, A. Magliocca, S. Quattrucci, S. De Sanctis, F. Alatri, G. Mazzarella, L. De Pietro, C. Turino, E. Melillo, P. Buonpensiero, A. Di Pasqua, V. Raia Journal of Cystic Fibrosis Volume 14, Issue 2, Pages 203-210 (March 2015) DOI: 10.1016/j.jcf.2014.09.014 Copyright © 2014 European Cystic Fibrosis Society. Terms and Conditions
Fig. 1 Study timeline. Journal of Cystic Fibrosis 2015 14, 203-210DOI: (10.1016/j.jcf.2014.09.014) Copyright © 2014 European Cystic Fibrosis Society. Terms and Conditions
Fig. 2 Flow diagram of study population. Journal of Cystic Fibrosis 2015 14, 203-210DOI: (10.1016/j.jcf.2014.09.014) Copyright © 2014 European Cystic Fibrosis Society. Terms and Conditions
Fig. 3 Changes from baseline of FEV1 at each study visit measured in children as liter with standard error (A) and percentage predicted with standard error (B); in adults as liter with standard error (C) and percentage predicted with standard error (D); in patients with FEV1% <81% as liter with standard error (E) and percentage predicted with standard error (F); in patients with FEV1% >81% as liter with standard error (G) and percentage predicted with standard error (H). Dark gray: glutathione; light gray: placebo. Journal of Cystic Fibrosis 2015 14, 203-210DOI: (10.1016/j.jcf.2014.09.014) Copyright © 2014 European Cystic Fibrosis Society. Terms and Conditions