Effect of misoprostol moistened with normal saline and acetic acid for second-trimester pregnancy termination.
Not Applicable
- Conditions
- Induce abortion of second trimester of pregnancy.Other and unspecified failed attempted abortion, without complication
- Registration Number
- IRCT2017082635898N1
- Lead Sponsor
- Vice chancellor for research, Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- Not specified
Inclusion Criteria
inclusion: pregnant women at 14 to 26 weeks of pregnancy who admitted for induced abortion with vaginal misoprostol.
exclusion criteria :not respond to misoprostol;start of spontaneous abortion;
contraindication of medical termination like previa placenta;prostaglandin contraindication like hyper sensivity,asthma, glucoma, cardiovascular disease.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Success in termination of pregnancy at first 24 hours. Timepoint: Every 4 hour from intervention. Method of measurement: Questionnaire, hour.;Success in termination of pregnancy after first dose. Timepoint: Every 4 hours from intervention. Method of measurement: Questionnaire, hour.
- Secondary Outcome Measures
Name Time Method Induction interval to delivery. Timepoint: During 72 hours from intervention. Method of measurement: Questionnaire, hour.;Dose of misoprostol used to termination. Timepoint: During 72 hour from intervention. Method of measurement: Questionnaire.;Side effects, nausa, vomiting, shaking. Timepoint: During 48 hours from intervention. Method of measurement: Questionnaire, check list.