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

Phase 2

• Conditions: Fibroidsuterine fibroma; Misoprostol; bleeding volume; abdominal hysterectomy

• Registration Number: TCTR20150924001
• Lead Sponsor: shahid sadoughi university of medical sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2015-09-24
• Study Completion: 2015-09-30
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending (Not yet recruiting)
• Sex: Female
• Target Recruitment: 40

Inclusion Criteria

patients hospitalized due to uterine myoma in Gynecology ward of Shahid Sadoughi hospital in 2012, candidate for abdominal hysterectomy

Exclusion Criteria

chemoterapy

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Hb levels 8 and 30 hours following surgery micro gram

Secondary Outcome Measures

Name	Time	Method
Age, previous operations and BMI before surgery nil