labour induction. Failed induction of labor
Conditions
Interventions
Intervention 1: The first intervention group of vaginal misoprostol will receive 25 micrograms of misoprostol (manufactured by Aria Pharmaceutical Company) vaginally. Intervention 2: The second interv
Sponsors
Kermanshah University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Monogamous Pregnancy above 37 weeks bishop's score less than/equal to 4 Cephalic presentation live fetus The weight of the fetus is less than 4 kilograms and the amniotic fluid index is more than 5
Exclusion criteria
Exclusion criteria: Mothers who have contraindications for taking misoprostol (active cardiopulmonary disease, history of previous cesarean section, or history of major uterine surgery such as myomectomy and uterine reconstruction surgery).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Duration of labor. Timepoint: End of study. Method of measurement: Based on the time measured from induction of labor to final delivery.;Nausea. Timepoint: During the study. Method of measurement: Ask the patient.;Fever. Timepoint: During the study. Method of measurement: Using a thermometer.;Chills. Timepoint: During the study. Method of measurement: Ask the patient. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMahdis Akrami
Kermanshah University of Medical Sciences
Outcome results
None listed