sublingual misoprostol 25 µg and oral misoprostol 50 µg on reducing post-term pregnancy
Early Phase 1
Recruiting
- Conditions
- termination of pregnancy.Medical abortion
- Registration Number
- IRCT20191208045653N1
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 140
Inclusion Criteria
Maximum gestational age of 40 weeks
pregnant women
Prime Grave
Single pregnancy
Cephalic display
Having normal amniotic fluid (AFI greater than or equal to 5 cm)
Bishop Score less than 8
Maternal age between 18 and 40 years
Exclusion Criteria
History of medical and midwifery disease
Diabetes
Preeclampsia
History of stillbirth
Opt out of the study
Improper use of medication
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of Cervical Preparation to Delivery. Timepoint: After Intervention. Method of measurement: Time.
- Secondary Outcome Measures
Name Time Method Fetal heart monitoring. Timepoint: After intervention. Method of measurement: Cardiac monitoring device.