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NCT00375986 · ClinicalTrials.gov registry record · NA
A Comparison of Manual vs. Spontaneous Removal of the Placenta at Cesarean Section
A NA study of Pregnancy and Cesarean Section, sponsored by University of Rochester.
- Completed
- Registry status
- NA
- Development phase
- 150
- Enrollment target
- 1
- Study location
NCT00375986 is a NA study of Pregnancy and Cesarean Section that has completed, run by University of Rochester. The registered enrollment target is 150 participants, below the 872-participant average among 191 other Pregnancy trials with a reported enrollment target (83% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00375986, a NA study of Pregnancy and Cesarean Section, has completed, sponsored by University of Rochester.
- COMPLETED
- Registry status
- NA
- Development phase
- 150 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to determine if there are differences in operative blood loss with manual vs. spontaneous removal of the placenta during cesarean section.
Conditions Studied
Interventions
- PROCEDURE Manual placental removal at Cesarean delivery
- PROCEDURE Spontaneous placental removal at Cesarean delivery
Study Locations (1)
New York
- Strong Memorial Hospital - Rochester
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 150 participants |
| Start Date | 2006-09 |
| Est. Completion | 2007-06 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00375986
The ClinicalTrials.gov registry entry for NCT00375986 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 150 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 872-participant average among 191 other Pregnancy trials with a reported enrollment target (83% lower). The listed sponsor is University of Rochester, which has 636 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Pregnancy appearing as the primary indexed condition, and to 2 interventions - of which Manual placental removal at Cesarean delivery is the first listed.
NCT00375986 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.
Frequently Asked Questions
What is clinical trial NCT00375986 about?
NCT00375986 is a clinical study titled "A Comparison of Manual vs. Spontaneous Removal of the Placenta at Cesarean Section". The purpose of this study is to determine if there are differences in operative blood loss with manual vs. spontaneous removal of the placenta during cesarean section.
What is the current status of trial NCT00375986?
This trial is currently completed. It is a NA study. The enrollment target is 150 participants. The study started on 2006-09. Estimated completion is 2007-06.
What conditions does trial NCT00375986 study?
This clinical trial studies the following conditions: Pregnancy, Cesarean Section.
What interventions are being tested in trial NCT00375986?
The interventions under investigation include: Manual placental removal at Cesarean delivery (PROCEDURE), Spontaneous placental removal at Cesarean delivery (PROCEDURE).
Who is sponsoring clinical trial NCT00375986?
This trial is sponsored by University of Rochester, which has 636 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00375986 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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Read our methodology - how this data is sourced, computed, and verified.
Related
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