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PDIUC Protocol for Placental Accreta — PDIUC  

Placenta Accreta Clinical Trial

Official title:
Preplacental Delivery Intervention for Uterine Conservation Protocol: a Novel Approach for Management of Placenta Accreta

Clinical Trial Summary

The aim of this study is to evaluate a novel protocol to conserve the uterus during Cesarean delivery indicated for placenta accreta.

Clinical Trial Description

Placenta accreta is a morbid obstetric condition that describes variable non-physiologic invasion of the placenta into the the uterine wall. The incidence of placenta accreta, as a serious cause of postpartum hemorrhage, has substantially increased secondary to increase the rate of Cesarean delivery. Placenta accreta is primarily managed by peripartum hysterectomy prior to delivery of the placenta to avoid uncontrolled bleeding. However, in addition to the surgical risks, hysterectomy is psychologically morbid to many women particularly younger women and women with low parity. Therefore, several conservative options were studied to provide an alternative for hysterectomy in these women. Our study is designated to evaluate a proposed protocol of multi-step interventions to reduce the anticipated amount of bleeding prior to delivery of the placenta. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03273569
Study type Interventional
Source Assiut University
Contact Sherif Shazly, MBBCh, MSc
Phone +15075131392
Email sherify2k2@gmail.com
Status Not yet recruiting
Phase N/A
Start date October 1, 2017
Completion date June 1, 2018
View Details
See also
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