Status:
ACTIVE_NOT_RECRUITING
Comparison Between Vaginal Misoprostol Gel and Oral Misoprostol Solution in Induction of Labor
Lead Sponsor:
Hagar Muhammad Abdulfattah Muhammad
Conditions:
Cervical Ripening and Induction of Labor
Eligibility:
FEMALE
18-40 years
Phase:
EARLY_PHASE1
Brief Summary
The goal of this clinical trial is to study the efficacy of vaginal versus oral misoprostol solution in cervical ripening for induction of labor. The main questions it aims to answer is : is Vaginal ...
Eligibility Criteria
Inclusion
- Women with a singleton pregnancy.
- Cephalic presentation.
- Age range: 18-40 years.
- Gestational age between 36 and 42 weeks.
- Intact fetal membranes.
- Absence of spontaneous uterine contractions.
- Non favorable cervix (Bishop score ≤ 5).
- A reactive non stress test in case of positive fetal life.
Exclusion
- History of cesarean section or uterine scars
- Grand Multipara P ≥5
- Known fetal non-cephalic presentation
- Any known allergy to misoprostol.
- Multiple pregnancy
- Contraindication to vaginal delivery.
Key Trial Info
Start Date :
February 26 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
September 1 2025
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT06874049
Start Date
February 26 2025
End Date
September 1 2025
Last Update
March 13 2025
Active Locations (1)
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1
Ain Shams university Maternity Hospital
Cairo, Egypt