CFDB - Cystic Fibrosis DataBase

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Aztreonam for inhalation solution (AZLI) in patients with cystic fibrosis, mild lung impairment, and P. aeruginosa.

primary studies  published RCT

Details
  • 2011
  • Wainwright CE

Effect of bronchoalveolar lavage-directed therapy on Pseudomonas aeruginosa infection and structural lung injury in children with cystic fibrosis: a randomized trial.

primary studies  published RCT

Details
  • 2011
  • Wainwright CE

Effect of VX-770 in persons with cystic fibrosis and the G551D-CFTR mutation.

primary studies  published RCT

Details
  • 2010
  • Accurso FJ

Hypertonic saline improves the LCI in paediatric patients with CF with normal lung function.

primary studies  published RCT

Details
  • 2010
  • Amin R

Hyaluronic acid improves "pleasantness" and tolerability of nebulized hypertonic saline in a cohort of patients with cystic fibrosis.

primary studies  published RCT

Details
  • 2010
  • Buonpensiero P

Absorptive clearance of DTPA as an aerosol-based biomarker in the cystic fibrosis airway.

primary studies  published RCT

Details
  • 2010
  • Corcoran TE

Inhaled mannitol improves the hydration and surface properties of sputum in patients with cystic fibrosis.

primary studies  published RCT

Details
  • 2010
  • Daviskas E

Melatonin improves sleep and reduces nitrite in the exhaled breath condensate in cystic fibrosis--a randomized, double-blind placebo-controlled study.

primary studies  published RCT

Details
  • 2010
  • de Castro-Silva C

Efficacy and tolerability of a new formulation of pancrelipase delayed-release capsules in children aged 7 to 11 years with exocrine pancreatic insufficiency and cystic fibrosis: a multicenter, randomized, double-blind, placebo-controlled, two-period crossover, superiority study.

primary studies  published RCT

Details
  • 2010
  • Graff GR

Evaluation of a home telemonitoring service for adult patients with cystic fibrosis: a pilot study.

primary studies  published RCT

Details
  • 2010
  • Grzincich G