Sublingual and buccal misoprostol in the first trimester abortions
Phase 3
Recruiting
- Conditions
- Medical abortion of the first trimester.Medical abortion
- Registration Number
- IRCT20230617058504N1
- Lead Sponsor
- Iran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 300
Inclusion Criteria
Abortion indication in the first trimester (including legal abortion, missed abortion, incomplete induced abortion)
Signing informed consent
Exclusion Criteria
Allergy to misoprostol
Previous history of cesarean section
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Percentage of treatment failure. Timepoint: 24 hours post-intervention. Method of measurement: Evaluation of the complete excretion of the product of pregnancy through clinical history and examination and in case of uncertainty, through ultrasound.
- Secondary Outcome Measures
Name Time Method Misoprostol side effects. Timepoint: Immediately after , 6, 24 and 48 hours post-intervention. Method of measurement: Clinical history and examination.;Lenght of hospitalization. Timepoint: Time of discharge. Method of measurement: Based on the information of the medical records.