Optimization of Saturation Targets And Resuscitation Trial (OptiSTART)
Recruiting
N/A
Interventional Study
Premature Infants
Bronchopulmonary Dysplasia
Intraventricular Hemorrhage
Neurodevelopmental Outcomes
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 0 Minutes – 10 Minutes
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 700 (estimated)
- Sponsor
- University of Texas Southwestern Medical Center · Other
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About This Trial
This study is designed to answer one of the fundamental gaps in knowledge in the resuscitation of preterm infants at birth: What is the optimal target oxygen saturation (SpO2) range that increases survival without long-term morbidities? Oxygen (O2) is routinely used for the stabilization of preterm infants in the delivery room (DR), but its use is linked with mortality and several morbidities incl…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
-Neonates with OB gestational age 22-30 weeks
Exclusion Criteria:
* Prenatally diagnosed cyanotic congenital heart disease
* Prenatally diagnosed congenital diaphragmatic hernia
* Parents request no resuscitation
* If preductal saturations can not be measured by 3 minutes afte…
Contacts