Randomized Clinical Trial of Early Delivery in Fetal Gastroschisis vs. Routine Care
Stopped early · Not applicable
Conditions studied: Gastroschisis
In brief
Primary objective: to test the hypothesis that elective early delivery will protect the fetal bowel from the deleterious intrauterine factors late in the pregnancy and will be associated with improved neonatal outcomes. Secondary objective: to introduce a standardized diagnostic, monitoring, and postnatal surgical management of infants with gastroschisis.
Key facts
- Study ID
- NCT01884324
- Run by
- Baylor College of Medicine
- People needed
- 21
- Starts
- 2013-06-01
- Expected to finish
- 2017-01-01
- Last updated by the study team
- 2017-07-13
Who can join
Age: 16 and older, up to 50. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Pregnant
- 16-50 years of age
- Prenatal diagnosis of fetal gastroschisis
- Less than 34 weeks and 0 days gestation
You may not qualify if…
- Greater than 34 weeks gestation
- 2. Fetus with massive gastroschisis defect that is not treatable after delivery
Where it is running
- Baylor College of Medicine — Houston, Texas, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.