Comparison of misoprostol and hypotensive anesthesia on blood loss during myomectomy

Phase 3

Recruiting

• Conditions: leiomyoma of uterus.; Intramural leiomyoma of uterus; D25.1

• Registration Number: IRCT20220930056059N1
• Lead Sponsor: Vice chancellor for Research, Tabriz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 November 2022

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 94

Inclusion Criteria

Ages 18-48
Willingness to enter the study
Having an indication for abdominal myomectomy

Exclusion Criteria

Anemia (hemoglobin less than 10)
Allergy to misoprostol
Cardiac and pulmonary diseases
Use of anticoagulant drugs

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Blood loss during surgery. Timepoint: During and after surgery. Method of measurement: Volume of blood in suction & bloody sponge count.

Secondary Outcome Measures

Name	Time	Method
Vital Signs. Timepoint: Before the intervention, then every 15 minutes until the end of the surgery. Method of measurement: Patient monitoring.;Hemoglobin count . Timepoint: Hemoglobin before & 6 houre & 12 houerafter operation. Method of measurement: Blood examination.