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NCT02659605 · ClinicalTrials.gov registry record · NA
Cord Clamping Level Above or Below Mother's Perineum
A NA study of Delayed Cord Clamping and Pre-Term Birth, sponsored by The University of Texas Health Science Center, Houston.
- Completed
- Registry status
- NA
- Development phase
- 103
- Enrollment target
- 1
- Study location
NCT02659605 is a NA study of Delayed Cord Clamping and Pre-Term Birth that has completed, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 103 participants. The trial reports 1 study location across 1 state.
The verdict
NCT02659605, a NA study of Delayed Cord Clamping and Pre-Term Birth, has completed, sponsored by The University of Texas Health Science Center, Houston.
- COMPLETED
- Registry status
- NA
- Development phase
- 103 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to determine if delayed cord clamping above the perineum has an effect on neonatal hematocrit when compared to delayed cord clamping below the perineum in pre-term spontaneous vaginal deliveries.
Conditions Studied
Interventions
- PROCEDURE Delayed cord clamping above the perineum
- PROCEDURE Delayed cord clamping below the perineum
Study Locations (1)
Texas
- Children's Memorial Hermann Hospital - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 103 participants |
| Start Date | 2016-01 |
| Est. Completion | 2017-02 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02659605
The ClinicalTrials.gov registry entry for NCT02659605 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 103 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Delayed Cord Clamping appearing as the primary indexed condition, and to 2 interventions - of which Delayed cord clamping above the perineum is the first listed.
NCT02659605 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT02659605 about?
NCT02659605 is a clinical study titled "Cord Clamping Level Above or Below Mother's Perineum". The purpose of this study is to determine if delayed cord clamping above the perineum has an effect on neonatal hematocrit when compared to delayed cord clamping below the perineum in pre-term spontaneous vaginal deliveries.
What is the current status of trial NCT02659605?
This trial is currently completed. It is a NA study. The enrollment target is 103 participants. The study started on 2016-01. Estimated completion is 2017-02.
What conditions does trial NCT02659605 study?
This clinical trial studies the following conditions: Delayed Cord Clamping, Pre-Term Birth.
What interventions are being tested in trial NCT02659605?
The interventions under investigation include: Delayed cord clamping above the perineum (PROCEDURE), Delayed cord clamping below the perineum (PROCEDURE).
Who is sponsoring clinical trial NCT02659605?
This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02659605 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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