Home › Bronchopulmonary Dysplasia › NCT04270045
Forced Oscillometry in Infants With Bronchopulmonary Dysplasia
RecruitingObservational study
Who can join
All ages · All sexes
Full eligibility criteria
Inclusion Criteria: Preterm Cohort: * Premature infants with BPD who are in room air based on the (per NICHD definition) * Premature infants with BPD who are receiving low flow O2 support and able to maintain normal spO2 in Room air for brief period ( up to 3 minutes) Term Cohort without pulmonary disease * Infants \>36 weeks gestational age without pulmonary disease * Infants \< 4 weeks of age Outpatient Cohort: * Former preterm infants \< 32 weeks at birth * Those with BPD based on NIH 2001 definition * Seen prior to 2 years of age Exclusion Criteria: * Infants with BPD requiring invasive or non-invasive positive pressure ventilation * Infants with BPD who have associated genetic diagnosis or major congenital anomalies.
About the study
The purpose of this study is to use forced oscillometry technique (FOT) to measure pulmonary mechanics and function in in term infants and premature infants with bronchopulmonary dysplasia (BPD)
What is being tested
- Non-invasive forced airway oscillometry (device)
Sponsor: Winston Manimtim · Participants: 80 · Started: Feb 6, 2020
Contact the study team
- Winston M Manimtim, MD, FAAP · Phone: (816) 234-3592
- Miah A Ruffin · Phone: (816)731-7443
Official record on ClinicalTrials.gov — NCT04270045
Locations in the U.S.
| Missouri | Children's Mercy Hospital, Kansas City |
Conditions
From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.