The effect of misoprostol with folley catheter (traction) & Rising induction in second trimester terminatio
Not Applicable
- Conditions
- Abortion.Medical abortion
- Registration Number
- IRCT201103146066N1
- Lead Sponsor
- Vice chancellor for research, Hamedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 72
Inclusion Criteria
All pregnant women admitted for trmination of pregnancy in second trimester with medical indications and don`t have any contraindication for study intervention; such as heart failure, severe anemia, using high dose corticosteroids and history of adrenal failure or allergic reaction
Exclusion criteria:
All women are not in mid-trimester and they do not accept to participate in the study
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time from beginig the induction to delivery. Timepoint: Time of beginig the induction till 48 hours. Method of measurement: Hour.;Need for curettage. Timepoint: 30 minute till one hour after delivery. Method of measurement: Standard teatment protocol.
- Secondary Outcome Measures
Name Time Method The days of admission in hospital. Timepoint: Study period. Method of measurement: Medical documents reports.;Possible side-effect. Timepoint: Study period. Method of measurement: Medical documents reports.