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NCT01884324 · ClinicalTrials.gov registry record · NA
Randomized Clinical Trial of Early Delivery in Fetal Gastroschisis vs. Routine Care
A NA study, sponsored by Baylor College of Medicine.
- Terminated
- Registry status
- NA
- Development phase
- 21
- Enrollment target
NCT01884324 is a NA study that was terminated before completion, run by Baylor College of Medicine. The registered enrollment target is 21 participants.
The verdict
NCT01884324, a NA study, was terminated before completion, sponsored by Baylor College of Medicine.
- TERMINATED
- Registry status
- NA
- Development phase
- 21 participants
- Enrollment target
Study Summary
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.
Interventions
- OTHER Early Delivery
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 21 participants |
| Start Date | 2013-06 |
| Est. Completion | 2017-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01884324
The ClinicalTrials.gov registry entry for NCT01884324 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 21 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Baylor College of Medicine, which has 616 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Early Delivery is the first listed.
NCT01884324 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01884324 about?
NCT01884324 is a clinical study titled "Randomized Clinical Trial of Early Delivery in Fetal Gastroschisis vs. Routine Care". 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 po...
What is the current status of trial NCT01884324?
This trial is currently terminated. It is a NA study. The enrollment target is 21 participants. The study started on 2013-06. Estimated completion is 2017-01.
What interventions are being tested in trial NCT01884324?
The interventions under investigation include: Early Delivery (OTHER).
Who is sponsoring clinical trial NCT01884324?
This trial is sponsored by Baylor College of Medicine, which has 616 total clinical trials registered on ClinicalTrials.gov.
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