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NCT03150641 · ClinicalTrials.gov registry record · NA
Delayed Cord Clamping at Term Cesarean
A NA study of Cesarean Delivery and Delayed Cord Clamping, sponsored by Columbia University.
- Completed
- Registry status
- NA
- Development phase
- 113
- Enrollment target
- 1
- Study location
NCT03150641 is a NA study of Cesarean Delivery and Delayed Cord Clamping that has completed, run by Columbia University. The registered enrollment target is 113 participants, below the 3,472-participant average among 10 other Cesarean Delivery trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state.
The verdict
NCT03150641, a NA study of Cesarean Delivery and Delayed Cord Clamping, has completed, sponsored by Columbia University.
- COMPLETED
- Registry status
- NA
- Development phase
- 113 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this research study is to find out how delaying cutting the umbilical cord until one minute after delivery of the baby during a cesarean impacts the amount of blood the mother loses during surgery. The study will also examine the benefits to the newborn from delayed cord clamping during cesarean.
Conditions Studied
Interventions
- PROCEDURE Umbilical cord clamping
Study Locations (1)
New York
- Columbia University Irving Medical Center - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 113 participants |
| Start Date | 2017-09-18 |
| Est. Completion | 2018-03-31 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03150641
The ClinicalTrials.gov registry entry for NCT03150641 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 113 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 3,472-participant average among 10 other Cesarean Delivery trials with a reported enrollment target (97% lower). The listed sponsor is Columbia University, which has 958 total studies on file at ClinicalTrials.gov.
The record links to 4 conditions, with Cesarean Delivery appearing as the primary indexed condition, and to 1 intervention - of which Umbilical cord clamping is the first listed.
NCT03150641 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.
Frequently Asked Questions
What is clinical trial NCT03150641 about?
NCT03150641 is a clinical study titled "Delayed Cord Clamping at Term Cesarean". The purpose of this research study is to find out how delaying cutting the umbilical cord until one minute after delivery of the baby during a cesarean impacts the amount of blood the mother loses during surgery. The study will also examine the benefits to the newborn from delayed cord clamping duri...
What is the current status of trial NCT03150641?
This trial is currently completed. It is a NA study. The enrollment target is 113 participants. The study started on 2017-09-18. Estimated completion is 2018-03-31.
What conditions does trial NCT03150641 study?
This clinical trial studies the following conditions: Cesarean Delivery, Delayed Cord Clamping, Maternal Blood Loss, Neonatal Health.
What interventions are being tested in trial NCT03150641?
The interventions under investigation include: Umbilical cord clamping (PROCEDURE).
Who is sponsoring clinical trial NCT03150641?
This trial is sponsored by Columbia University, which has 958 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03150641 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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