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NCT05979181 Clinical Trial

Peripartum Cesarean Hysterectomy for Placenta Percreta

Placenta Accreta Clinical Trial

Official title:
Peripartum Cesarean Hysterectomy for Placenta Percreta: a Retrospective Analysis of Cases With and Without Extrauterine Disease

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05979181
Other study ID # R.23.06.2211
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 20, 2018
Est. completion date February 17, 2023

Study information
Verified date July 2023
Source Mansoura University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to address the possible preoperative determinants of extrauterine diseases in cases of placenta previa percreta and to compare the operative and postoperative characteristics of cases with and without extrauterine disease.

Description:

This will be a retrospective study of the data of women who underwent cesarean hysterectomy on placenta previa percreta who were classified as Federation of Gynecology and Obstetrics (FIGO) grade 3. Women without extrauterine disease (FIGO grade 3a) will be compared to women with extrauterine disease (FIGO grades 3b and 3c)

Recruitment information / eligibility
Status Completed
Enrollment 73
Est. completion date February 17, 2023
Est. primary completion date February 17, 2023
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria: - Women who underwent cesarean hysterectomy on placenta previa percreta (FIGO grade 3). Exclusion Criteria: - Medical conditions complicating pregnancy. - Blood diseases or bleeding tendencies

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Cesarean hysterectomy
Cesarean hysterectomy due to placenta previa percreta with no extrauterine disease (FIGO grade 3a) or with extrauterine disease (FIGO grades 3b and 3c)

Locations
Country Name City State
Egypt Mansoura University Hospital Mansoura Dakahlia

Sponsors (1)
Lead Sponsor Collaborator
Mansoura University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Estimated amount of intraoperative blood loss Calculated amount of blood loss during the operation From start to end of operation
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