Myomectomy During CS: A Retrospective Cohort Study

Completed

• Conditions: Cesarean Section; Uterine Fibroid
• Interventions: Procedure: Myomectomy

• Registration Number: NCT03270605
• Lead Sponsor: Mansoura University

Brief Summary

To evaluate the value of myomectomy during delivery by cesarean section (CS) in pregnant women with uterine fibroids.

Detailed Description

Not available

Study Timeline

• Study Start: 2015-01-01
• Study First Submitted: 2017-08-31
• Study First Submitted QC: 2017-08-31
• Study First Posted: 2017-09-01
• Primary Completion: 2019-12-31
• Study Completion: 2019-12-31
• Status Verified: 2020-08
• Last Update Submitted: 2020-08-28
• Last Update Posted: 2020-09-01

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 178

Inclusion Criteria

• Women who underwent elective CS with presence of uterine fibroid during the index pregnancy documented antenatal and at surgery

Exclusion Criteria

• Antepartum hemorrhage
• Blood diseases or bleeding tendencies.
• Medical conditions complicating pregnancy.
• Performed another surgical procedure at CS other than myomectomy.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
CS with myomectomy	Myomectomy	Women having uterine myoma with pregnancy and subjected to myomectomy during delivery by CS

Primary Outcome Measures

Name	Time	Method
Deficit in hemoglobin level	24 hours	Preoperative hemoglobin minus postoperative hemoglobin level (in gm/dl)

Secondary Outcome Measures

Name	Time	Method
Operative time	3 hours	Time to complete the procedure
Postoperative hospital stay period	7 days	Time from the end of operation to discharge from hospital