Prophylactic Minimally Invasive Surfactant Evaluation (NCT06007547)
๐ฉบ Plain-English Summary (8th-Grade Level)
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?
Who can join: Review the eligibility criteria below.
Location: Northshore University Healthsystem โ Evanston, Illinois
Age range: Not specified to 15 Minutes
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (1 Sites)
- Northshore University Healthsystem โ Evanston, Illinois
๐ Contact the Study Coordinator
Phone: (847) 570-2920
Email: mderrick@northshore.org
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Respiratory Distress Syndrome, Newborn
- Measuring Diaphragm Electrical Activity in Neonates Using a Smaller Inter-electrode Distance โ Toronto, Ontario
- Echography-guided Surfactant THERapy (ESTHER) For Preterm Infants With Respiratory Failure โ Hartford, Connecticut
- Predicting the Need for Prolonged Respiratory Support in Neonates Delivered in a Lower-Level NICU Setting โ Rochester, Minnesota
- Utilization of Lung Ultrasound Score in Decision for Minimally Invasive Surfactant Administration โ Hackensack, New Jersey
Explore by condition: All Respiratory Distress Syndrome, Newborn clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.