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Efficacy Study of Random Placenta Margin Incision to Treat Complete Placenta Previa

NCT02695069 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2017-11-13

No results posted yet for this study

Summary

The purpose of this study is to assess the efficacy of random placenta margin incision for hemorrhage control during cesarean section of complete placenta previa pregnancies.

Conditions

  • Complete Placenta Previa

Interventions

PROCEDURE

Random Placenta Margin Incision

A random hysterotomy incision is done in the placenta margin. To precisely determine the placental location and the edge of the placenta, preoperative ultrasonography is used in determining the optimal place for the uterine incision.

Sponsors & Collaborators

  • Maternal and Child Health Hospital of Foshan

    lead OTHER

Principal Investigators

  • Zhengping Liu, MD · Maternal and Child Health Hospital of Foshan

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-01-31
Primary Completion
2017-03-31
Completion
2017-04-30

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02695069 on ClinicalTrials.gov