Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Completed · Phase 2/Phase 3
Conditions studied: Infant, Newborn, Infant, Low Birth Weight, Infant, Small for Gestational Age, Infant, Premature, Bronchopulmonary Dysplasia
In brief
The purpose of this study is to compare the efficacy of two surfactants, Exosurf Neonatal (Burroughs Wellcome Co.) and Survanta (Ross Laboratories), for the treatment of neonatal respiratory distress syndrome.
Key facts
- Study ID
- NCT01203358
- Run by
- NICHD Neonatal Research Network
- People needed
- 617
- Starts
- 1991-01-01
- Expected to finish
- 1992-01-01
- Last updated by the study team
- 2019-03-22
Who can join
Age: any, up to 0. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Newborn infants weighing 501 to 1500 gm with respiratory distress syndrome were receiving assisted ventilation with 30% oxygen or more
You may not qualify if…
- Less than 6 hours of age
Where it is running
- Stanford University — Palo Alto, California, United States
- Yale University — New Haven, Connecticut, United States
- George Washington University — Washington D.C., District of Columbia, United States
- University of Miami — Miami, Florida, United States
- Emory University — Atlanta, Georgia, United States
- Indiana University — Indianapolis, Indiana, United States
- Wayne State University — Detroit, Michigan, United States
- University of New Mexico — Albuquerque, New Mexico, United States
- Cincinnati Children's Medical Center — Cincinnati, Ohio, United States
- Case Western Reserve University, Rainbow Babies and Children's Hospital — Cleveland, Ohio, United States
- University of Tennessee — Memphis, Tennessee, United States
- University of Texas Southwestern Medical Center at Dallas — Dallas, Texas, United States
- University of Vermont — Burlington, Vermont, United States
Full record on ClinicalTrials.gov
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