Effect of single rectal dose of Misoprostol prior to abdominal hysterectomy in women with symptomatic leiomyoma: a randomized double blind clinical trial

Phase 3

Active, not recruiting

• Conditions: abdominal hysterectomybleeding volumeMisoprostol; Misoprostol; bleeding volume; abdominal hysterectomy

• Registration Number: TCTR20151011001
• Lead Sponsor: none

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2015-10-10
• Study Start: 2015-10-11
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Active, not recruiting
• Sex: Female
• Target Recruitment: 40

Inclusion Criteria

uterine myoma
candidate for abdominal hysterectomy

Exclusion Criteria

emergency condition

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
bleeding 0 litr

Secondary Outcome Measures

Name	Time	Method
age 0 year