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NCT00711451 · ClinicalTrials.gov registry record · NA
Manual and Expressed Placental Removal at Cesarean Delivery and Its Effects on Various Cardiac Indices
A NA study, sponsored by Corewell Health East.
- Terminated
- Registry status
- NA
- Development phase
- 19
- Enrollment target
NCT00711451: Clinical Trial NA study, sponsored by Corewell Health East.
NCT00711451 is a NA study that was terminated before completion, run by Corewell Health East. The registered enrollment target is 19 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00711451, a NA study, was terminated before completion, sponsored by Corewell Health East.
- TERMINATED
- Registry status
- NA
- Development phase
- 19 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate whether manual removal of the placenta during a cesarean delivery results in higher changes in the resistance of blood flow throughout the body, also called systemic vascular resistance (SVR)
Interventions
- BEHAVIORAL Manual removal
- PROCEDURE Expressed removal
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 19 participants |
| Start Date | 2008-07 |
| Est. Completion | 2012-01 |
| Phase | NA |
Why NCT00711451 stopped before completion
NCT00711451 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 19 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).
The record links to 0 conditions, and to 2 interventions - of which Manual removal is the first listed.
NCT00711451 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00711451 about?
NCT00711451 is a clinical study titled "Manual and Expressed Placental Removal at Cesarean Delivery and Its Effects on Various Cardiac Indices". The purpose of this study is to evaluate whether manual removal of the placenta during a cesarean delivery results in higher changes in the resistance of blood flow throughout the body, also called systemic vascular resistance (SVR)
What is the current status of trial NCT00711451?
This trial is currently terminated. It is a NA study. The enrollment target is 19 participants. The study started on 2008-07. Estimated completion is 2012-01.
What interventions are being tested in trial NCT00711451?
The interventions under investigation include: Manual removal (BEHAVIORAL), Expressed removal (PROCEDURE).
Who is sponsoring clinical trial NCT00711451?
This trial is sponsored by Corewell Health East, which has 106 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00711451's enrollment target sits among peer trials
19 1861st of 2000 higher than 138 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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