The effect of vaginal Evening Primrose Oil capsule versus placebo on cervical ripening and delivery outcomes in nulliparous wome
Phase 2
- Conditions
- Delivery outcomes.Encounter for supervision of other normal pregnancy, third trimesterZ34.83
- Registration Number
- IRCT20120215009014N231
- Lead Sponsor
- Hamedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 50
Inclusion Criteria
Age of 18 to 45 years;
Nulliparous;
Cephalic presentation of embryo and alive with normal patterns of embryonic heart rate;
Embryonic weight of 2500 to 3500 g;
Gestational age of 38 to 39 weeks;
Bishop score of 4 or lower
Exclusion Criteria
Sensitivity of herbal medications;
Amniotic fluid disorder;
Preeclampsia;
Diabetes;
Placenta aberration;
Placenta Previa;
Indication of cesarean
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Cervical ripening. Timepoint: During delivery. Method of measurement: With physical examination.;Neonate Apgar score. Timepoint: In the first and fifth minutes after delivery. Method of measurement: With physical examination.
- Secondary Outcome Measures
Name Time Method