Prophylactic Minimally Invasive Surfactant Evaluation

Description

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?

Conditions

Respiratory Distress Syndrome, Newborn, Premature Birth

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Study Overview

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Study Details

Study overview

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?

Prophylactic Minimally Invasive Surfactant Evaluation

Prophylactic Minimally Invasive Surfactant Evaluation

Condition
Respiratory Distress Syndrome, Newborn
Intervention / Treatment

-

Contacts and Locations

Evanston

Northshore University Healthsystem, Evanston, Illinois, United States, 60201

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.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Gestational age \<30 weeks
  • * Antenatal consent from Parent
  • * Congenital anomalies
  • * Alternate cause of respiratory distress

Ages Eligible for Study

to 15 Minutes

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

NorthShore University HealthSystem,

Matthew Derrick, MBBS, PRINCIPAL_INVESTIGATOR, Northshore Univ Healthsystem

Study Record Dates

2027-07-31