Cystic Fibrosis
Conditions
Keywords
ztr, transfer impedance, cystic fibrosis, pulmonary function test, pft
Brief summary
This study aims to determine whether respiratory system transfer impedance (Ztr) may fill an important clinical function by providing a reproducible, valid, and sensitive measure of airway obstruction in people with CF.
Interventions
None listed
Sponsors
Boston Children's Hospital
Study design
Observational model
CASE_ONLY
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
2 Years to 25 Years
Healthy volunteers
No
Inclusion criteria
* Between the ages of 2 to 25 Confirmed diagnosis of Cystic Fibrosis
Countries
United States
Outcome results
None listed