A Comparison of Manual vs. Spontaneous Removal of the Placenta at Cesarean Section

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

150 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-09-30

Study Completion Date

2007-06-30

Brief Summary

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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.

Detailed Description

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Patients undergoing scheduled cesarean deliveries are randomized to manual or spontaneous placental removal.

Conditions

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Pregnancy Cesarean Section

Keywords

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Cesarean delivery Placental removal Blood loss

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Blinding Strategy

NONE

Interventions

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Manual placental removal at Cesarean delivery

Intervention Type PROCEDURE

Spontaneous placental removal at Cesarean delivery

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* All term pregnant women 18 years of age and older undergoing scheduled cesarean delivery at Strong Memorial Hospital.

Exclusion Criteria

* Prematurity (\<37 weeks)
* Preoperative chorioamnionitis
* Vaginal delivery of fetus
* Emergency Cesarean Delivery
* Patient's OB not agreeable to participating in this study.

Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Principal Investigators

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Eva K. Pressman, MD

Role: PRINCIPAL_INVESTIGATOR

University of Rochester

Locations

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Strong Memorial Hospital

Rochester, New York, United States

Site Status

Countries

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United States

Other Identifiers

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00014248

Identifier Type: -

Identifier Source: org_study_id