Status:
UNKNOWN
PDIUC Protocol for Placental Accreta
Lead Sponsor:
Assiut University
Conditions:
Placenta Accreta
Eligibility:
FEMALE
18-40 years
Phase:
NA
Brief Summary
The aim of this study is to evaluate a novel protocol to conserve the uterus during Cesarean delivery indicated for placenta accreta.
Detailed 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 po...
Eligibility Criteria
Inclusion
- Women with diagnosis of placenta accreta (US or MRI based diagnosis)
- Women who decline hysterectomy
- Pregnancy at 28 weeks of gestation or beyond
- Women who accept to participate in the study
Exclusion
- Emergency Cesarean delivery (women with active bleeding)
- Women with cardiac diseases
- Women with coagulopathy
Key Trial Info
Start Date :
October 1 2017
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
June 1 2018
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT03273569
Start Date
October 1 2017
End Date
June 1 2018
Last Update
September 6 2017
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