← Eichor
Study identifier: NCT06007547 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Prophylactic Minimally Invasive Surfactant Evaluation

Condition: Respiratory Distress Syndrome, Newborn · Premature Birth  ·  Sponsor: Endeavor Health

PhasePhase 4
Planned participants200
Who can joinAll sexes, N/A to 15 Minutes
Healthy volunteersYes

About this study

The purpose of this study is to explore the question: Does prophylactic administration of exogenous surfactant in the delivery room, using a minimally-invasive technique, improve outcome in preterm infants 22-29 weeks' gestation compared to rescue treatment using the same technique?

This description comes directly from the study's public registry record.

Talk to the study team

Matthew Derrick, MBBS  ·  8475702920  ·  mderrick@northshore.org

Always discuss trial participation with your own doctor first.

Locations (1)

Northshore University HealthsystemEvanston, Illinois, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06007547