About this trial
The study population consists of term primigravida women undergoing induction of labor at a tertiary care referral center in Assiut, Egypt.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Singleton pregnancy
Disqualifiers
Previous uterine surgery (e.g., cesarean section, myomectomy)
Trial population
Participants include 88 primigravida women at ≥37 weeks of gestation, each with a singleton pregnancy in cephalic presentation. All participants present with medical or obstetric indications for induction of labor, such as post-dates, oligohydramnios, mild preeclampsia, or premature rupture of membranes. Exclusion criteria include prior uterine surgery, multiple pregnancies, malpresentation, placenta previa, vasa previa, non-reassuring fetal status at admission, or maternal infections such as active genital herpes and HIV. A carefully designed sample size calculation ensures adequate power, with a final cohort of 44 women per study arm.
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Rate of vaginal delivery
The proportion of women achieving vaginal delivery after induction of labor within 24 hours of initiation.
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: