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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: Completed NA study, sponsored by University of Mississippi Medical Center.
NCT01766908 is a NA study that has completed, run by University of Mississippi Medical Center. The registered enrollment target is 72 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
WE are seeking the length of time to delay cord clamping for various gestational age groups following vaginal or cesarean delivery in order to significantly improve primary outcome.
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 |
What the finished NCT01766908 record still lists
NCT01766908 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 72 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).
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 does not publish any study locations in the registry export this page uses.
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.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01766908's enrollment target sits among peer trials
72 1089th of 2000 higher than 899 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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