rectal misoprostol on intraoperative blood loss prior to abdominal myomectomy.
Phase 3
Recruiting
- Conditions
- myoma.Leiomyoma of uterus
- Registration Number
- IRCT20080826001096N5
- Lead Sponsor
- Guilan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 94
Inclusion Criteria
age between 18-50 years
5 or less symptomatic myoma
intramoral myoma based on sonography
A minimum of 4 cm in size of myoma (because no smaller than 4 cm can produce a lot of bleeding)
Exclusion Criteria
anemia (HB less than10)
allergy to Misoprostol (By asking questions such as skin sign, hives, rash, shortness of breath, coughing, chest pain after the previous use of Miso Prostol)
Cardiopulmonary diseases
Hemorrhage disorders
obese (Body Mass Index more than35)
Uncontrolled blood pressure despite drug use
uterine size more than 24 weeks
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method ength of stay in hospital. Timepoint: From admission to exit. Method of measurement: day.
- Secondary Outcome Measures
Name Time Method Postoperative hemoglobin and hematocrit. Timepoint: 4 and 24 hours after surgery. Method of measurement: blood test.;Blood loss. Timepoint: Intraoperative and postoperative. Method of measurement: On hemoglobin level and Severity of bleeding Total blood volume in the suction bottle + wet gauze and long gauze.