ower uterine compression sutures for the Treatment of Postpartum Hemorrhage due to Placenta Previa Complete centralis

Not Applicable

• Conditions: Condition 1: placenta previa. Condition 2: postpartum hemorrage.; Placenta praevia with haemorrhage; Postpartum haemorrhage

• Registration Number: IRCT2014040517081N1
• Lead Sponsor: Department of Obstetrics and Gynecology, Benha University Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 25

Inclusion Criteria

All patients had placenta previa complete centralis (25). The inclusion criteria are a gestation age of = 28 weeks and antepartum hemorrhage; intraoperative postpartum hemorrhage and discovery of a placenta previa; successful removal of the placenta

exclusion criteria: shock due to massive blood loss ,failure of successful removal of the placenta

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Treatment of postpartum hemorrage. Timepoint: at time of delivery. Method of measurement: observation.

Secondary Outcome Measures

Name	Time	Method
ormal patency of the uterine cavity. Timepoint: 6 months follow up. Method of measurement: sonohysterography.