RECRUITING

Forced Oscillometry in Infants with Bronchopulmonary Dysplasia

Conditions

Infant, Premature, Diseases Bronchopulmonary Dysplasia Respiratory Distress Syndrome

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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)

Official Title

Forced Oscillometry in Infants with Bronchopulmonary Dysplasia

Quick Facts

Study Start:2020-02-06

Study Completion:2026-03-31

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT04270045

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:Not specified

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:CHILD, ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
* 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 * Former preterm infants \< 32 weeks at birth * Those with BPD based on NIH 2001 definition * Seen prior to 2 years of age	* Infants with BPD requiring invasive or non-invasive positive pressure ventilation * Infants with BPD who have associated genetic diagnosis or major congenital anomalies.

Inclusion Criteria

Exclusion Criteria

* 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
* Former preterm infants \< 32 weeks at birth
* Those with BPD based on NIH 2001 definition
* Seen prior to 2 years of age

* Infants with BPD requiring invasive or non-invasive positive pressure ventilation
* Infants with BPD who have associated genetic diagnosis or major congenital anomalies.

Contacts and Locations

Study Contact

Winston M Manimtim, MD, FAAP

CONTACT

(816) 234-3592

wmmanimtim@cmh.edu

Cheri A Gauldin, RN

CONTACT

(816) 234-3596

cagauldin@cmh.edu

Study Locations (Sites)

Children's Mercy Hospital

Kansas City, Missouri, 64108

United States

Collaborators and Investigators

Sponsor: Winston Manimtim

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2020-02-06

Study Completion Date2026-03-31

Study Record Updates

Study Start Date2020-02-06

Study Completion Date2026-03-31

Terms related to this study

Additional Relevant MeSH Terms

Infant, Premature, Diseases
Bronchopulmonary Dysplasia
Respiratory Distress Syndrome