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Not yet recruitingNCT07860931Updated Oct 6, 2026

eCPAP Follow-up at School Age

An observational study in Lung Function, sponsored by Cynthia McEvoy. Not yet recruiting. Per ClinicalTrials.gov, last updated 2026-10-06.

Sponsored by Cynthia McEvoy · Observational

Updated Oct 6, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
95
Sex
All
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Study summary

The purpose of the study is to learn more about extended continuous positive airway pressure (eCPAP) in preterm infants that may be helpful for lung health. We are hoping to find out if eCPAP in stable preterm infants in the NICU results in long lasting improvements of lung function in school aged children.

Read the detailed description

This is an observational follow-up of former preterm children from the eCPAP radnomized controlled trial (NCT#04295564), a single-center study of eCPAP vs discontinue CPAP (dCPAP) in the neonatal intensive care unit at Oregon Health \& Science University (OHSU). All former preterm infants randomized in the parent study will be approached for reconsent into this follow-up study. We will determine if eCPAP for stable preterm infants in the NICU results in sustained improvement of lung function (primary outcome spirometry) and less respiratory morbidity (wheeze), at school age. We will determine if eCPAP in the NICU results in an airway tree with a larger cross- sectional area and greater lung volume at school age, which is associated with less respiratory morbidity. Additionally, we will obtain detailed biological data (DNA methylation and transcriptomics using nasal epithelium as a proxy for airway epithelium), to identify participants that share common molecular signatures (biological endotypes).

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Conditions studied

  • Lung Function

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Keywords

  • extended CPAP
  • eCPAP
  • Lung Function
  • NICU
  • Prematurity
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In context

Premature Birth

2,554 studies on the registry are indexed under Premature Birth; 498 are open to participants now.

This study's planned enrollment of 95 is below the median of 112 across 777 observational studies indexed under Premature Birth.

Browse Premature Birth studies →

Lead sponsor

Cynthia McEvoy is the lead sponsor of 3 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

This is an observational follow-up study of former preterm infants who participated in the randomized clinical trial extended CPAP "parent study."

Inclusion criteria

  • Children randomized in the parent study

Exclusion criteria

Exclusion Criteria:

  • None
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
95 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • eCPAP

    Group that was assigned to Extended CPAP (eCPAP)

    Other: Extended CPAP (eCPAP)

  • dCPAP

    Group that was assigned to discontinue CPAP (dCPAP)

Interventions

  • OtherExtended CPAP (eCPAP)

    Assigned to two extra weeks of CPAP

    Also known as: Treatment length

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What researchers measure

Primary outcomes

  1. Sustained improvement of lung function (functional outcomes)

    Determine if eCPAP for preterm infants in the NICU results in sustained improvement of lung function (primary outcome spirometry) and less respiratory morbidity (wheeze) at school age.

    Time frame: Between the ages of 6 and 8

Secondary outcomes

  1. Airway tree changes (structural outcomes)

    Determine via a single low dose high resolution computed tomography (HRCT) of the chest if eCPAP in the NICU results in an airway tree with a larger cross-sectional area and greater lung volume at school age, which is associated with less respiratory morbidity.

    Time frame: Between the ages of 6 and 8

  2. Molecular Endotypes

    Detailed biological data (DNA methylation and transcriptomics using nasal epithelium as a proxy for airway epithelium), will be used to identify patients that share common molecular signatures (biological endotypes).

    Time frame: Between the ages of 7 and 8

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Study locations

No study locations are listed for this record.

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References and documents

Publications

  • McEvoy CT, MacDonald KD, Go MA, Milner K, Harris J, Schilling D, Olson M, Tiller C, Slaven JE, Bjerregaard J, Vu A, Martin A, Mamidi R, Schelonka RL, Morris CD, Tepper RS. Extended Continuous Positive Airway Pressure in Preterm Infants Increases Lung Growth at 6 Months: A Randomized Controlled Trial. Am J Respir Crit Care Med. 2025 Apr;211(4):610-618. doi: 10.1164/rccm.202411-2169OC. PubMed 39977011 ↗

Individual participant data

Plan to share: Undecided

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Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 6, 2026
Show all 1 update
  1. Oct 6, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

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Registry details

Key details

Study ID
NCT07860931
Lead sponsor
Cynthia McEvoy
Collaborators
National Institutes of Health (NIH), National Heart, Lung, and Blood Institute (NHLBI), Indiana University
Responsible party
Cynthia McEvoy (MD, MCR, Professor of Pediatrics, Oregon Health and Science University) — Sponsor-investigator
First posted
Oct 6, 2026
Start date
Oct 2026 (estimated)
Primary completion
Dec 2032 (estimated)
Completion
Dec 2033 (estimated)
Last update
Oct 6, 2026

Study contacts

Cynthia McEvoy, MD, MCR
Contact
mcevoyc@ohsu.edu
503-494-0085
Kristin Milner, CMA, BS, CCRP
Contact
milner@ohsu.edu
971-278-3345
Cynthia McEvoy, MD, MCR
principal investigator · Oregon Health and Science University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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