Comparison of oral versus vaginal misoprostol for legal abortio
Phase 3
- Conditions
- Medical abortion.termination of pregnancy
- Registration Number
- IRCT2014110812789N9
- Lead Sponsor
- Vice Chancellor for Research, Kurdistan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 70
Inclusion Criteria
pregnant women who are candidates of pregnancy termination with the permission of legal Medicine.
Exclusion criteria : pregnant women who are breastfeeding, women with severe liver disease, chronic pulmonary disease, Mitral valve stenosis, history of allergy to prostaglandins, inflammatory disease of intestines, asthma, glaucoma, hypertension, and severe bleeding.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pregnancy Exertion. Timepoint: Beginning of the study, every 6 hours up to 36 hours. Method of measurement: dilatation of cervix-contraction and hemorrhage.
- Secondary Outcome Measures
Name Time Method Fever. Timepoint: Every one hour until the last dosage. Method of measurement: Clinical Examination.;Uterus perforation. Timepoint: Every one hour until the last dosage. Method of measurement: Clinical examination by Gynecology resident.;Amount of bleeding. Timepoint: The start of the intervention up to 36 hours. Method of measurement: Observation and clinical examination.