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.
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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

Vishal Kapadia, MD

2146483903

vishal.kapadia@utsouthwestern.edu

CONTACT

Shelby Unger, RN

2146483903

shelby.unger@utsouthwestern.edu

CONTACT