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NCT01766908 · ClinicalTrials.gov registry record · NA
Optimal Timing of Cord Clamping in Preterm Pregnancy Following Vaginal or Cesarean Delivery
A NA study, sponsored by University of Mississippi Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 72
- Enrollment target
NCT01766908 is a NA study that has completed, run by University of Mississippi Medical Center. The registered enrollment target is 72 participants.
The verdict
NCT01766908, a NA study, has completed, sponsored by University of Mississippi Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 72 participants
- Enrollment target
Study Summary
This is an experimental research study for pregnant women between 23 and 37 weeks age of gestation who will be having a baby sooner than term. This study is to learn if waiting 20, 40, or 60 seconds to clamp the umbilical cord after baby delivers will improve his/her outcome and overall health. Benefit to the baby may come by increasing the amount of blood in the baby's body, reducing the need for possible transfusion later, and possible prevention of other complications caused by too little blood in the baby. Possible reduction of cerebral palsy may be realized by a longer interval for cord clamping.
Interventions
- OTHER Clamp cord 20, 40 or 60 seconds following vaginal or cesarean delivery
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 72 participants |
| Start Date | 2012-12 |
| Est. Completion | 2014-06 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01766908
The ClinicalTrials.gov registry entry for NCT01766908 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 72 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Mississippi Medical Center, which has 96 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Clamp cord 20, 40 or 60 seconds following vaginal or cesarean delivery is the first listed.
NCT01766908 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01766908 about?
NCT01766908 is a clinical study titled "Optimal Timing of Cord Clamping in Preterm Pregnancy Following Vaginal or Cesarean Delivery". This is an experimental research study for pregnant women between 23 and 37 weeks age of gestation who will be having a baby sooner than term. This study is to learn if waiting 20, 40, or 60 seconds to clamp the umbilical cord after baby delivers will improve his/her outcome and overall health. Bene...
What is the current status of trial NCT01766908?
This trial is currently completed. It is a NA study. The enrollment target is 72 participants. The study started on 2012-12. Estimated completion is 2014-06.
What interventions are being tested in trial NCT01766908?
The interventions under investigation include: Clamp cord 20, 40 or 60 seconds following vaginal or cesarean delivery (OTHER).
Who is sponsoring clinical trial NCT01766908?
This trial is sponsored by University of Mississippi Medical Center, which has 96 total clinical trials registered on ClinicalTrials.gov.
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