Phase
Condition
Cystic Fibrosis
Lung Disease
Scar Tissue
Treatment
N/AClinical Study ID
Ages 1-30 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Age < 30 months
Diagnosis of CF based on clinical features consistent with CF as well as 1 of the 2following criteria: a) two sweat chlorides >60 mEq/L (by quantitative pilocarpineiontophoresis), b) genotype with 2 identifiable mutations consistent with CF.
Informed consent by parent or legal guardian
Exclusion
Exclusion Criteria:
Previous treatment with Pulmozyme
Hospitalization or treatment with IV antibiotics with 14 days of initial study visit
Acute intercurrent respiratory infection, defined as any of the following symptomswithin the preceding 48 hours: 1) fever > 38 degrees C, 2) new onset of coryza orother upper respiratory symptoms, 3) increase in cough, wheezing, or respiratory rate
History of adverse reaction to sedation
Oxyhemoglobin saturation <90% on room air
Severe upper airway obstruction as determined by site PI (severe laryngomalacia,markedly enlarged tonsils, significant snoring, diagnosed obstructive sleep apnea)
Hemodynamically significant congenital heart disease or diagnosed arrhythmias
History of hemoptysis
History of previous pulmonary air leak (pneumothorax)
Diagnosed seizure disorder necessitating current anticonvulsive therapy. A history offebrile seizures is not an exclusion criterion.
Use of Investigational drug(s) within 60 days or 5 half-lives of enrollment in thisstudy.
Known allergy to Chinese Hamster Ovary-derived biological products or any component ofthe placebo or active drug formulations.
Study Design
Study Description
Connect with a study center
Nationwide Children's Hospital
Columbus, Ohio 43205
United StatesSite Not Available

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