Determinants of Early Cystic Fibrosis Lung Disease

CompletedOBSERVATIONAL
Enrollment

61

Participants

Timeline

Start Date

May 8, 2018

Primary Completion Date

February 6, 2019

Study Completion Date

February 6, 2019

Conditions
Cystic Fibrosis in Children
Interventions
DIAGNOSTIC_TEST

Infant PFT

Assessed through the raised volume rapid thoracoabdominal compression technique and plethysmography

DIAGNOSTIC_TEST

Lung Clearance Index

The Lung Clearance Index is derived from the Multiple Breath Washout test. It is the cumulative exhaled volume (the volume of gas needed to wash out resident gas mixture out of the lungs) divided by the FRC. The FRC is the amount of air left in the lungs after normal exhalation.

DIAGNOSTIC_TEST

Passive tidal breathing

During quiet sleep, tidal breathing flow-volume curves are obtained. The tPEF/tE is calculated by taking the time it takes to reach peak expiratory flow divided by the total peak expiratory time.

Trial Locations (1)

46202

Riley Hospital for Children, Indianapolis

All Listed Sponsors
lead

Indiana University

OTHER

NCT03579173 - Determinants of Early Cystic Fibrosis Lung Disease | Biotech Hunter | Biotech Hunter