Condition 1: Abdominal pregnancy. Condition 2: (Induced) termination of pregnancy with other and unspecified complications. Abdominal pregnancy (Induced) termination of pregnancy with other and unspecified complications
Conditions
Interventions
Intervention 1: Intervention group: 50 micrograms of oral misoprostol for induction of labor. If no appropriate uterine contractions were observed, patients received 50 mg Misoprostol every four hour
Sponsors
Fasa University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Gestational age more than 42 weeks first and second pregnancy women over 18 years old singleton pregnancy, cervical closure (Bishop score greater than six)
Exclusion criteria
Exclusion criteria: Multiple pregnancies need for immediate cesarean section history of uterine scarring placenta previa vaginal bleeding more than normal postpartum bleeding heart, liver and kidney diseases history of sensitivity to Oxytocin, Misoprostol or prostaglandin analogues severe congenital anomalies in the fetus.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Delivery withing 48 hours after intervention. Timepoint: 48 hours after intervention. Method of measurement: Recording the number of patients with successful delivery within 48 hours.;Route of delivery. Timepoint: At time if delivery. Method of measurement: Recording the route of delivery (Cesarean or vaginal delivery).;Neonatal Apgar. Timepoint: 1 and 5 minutes after birth. Method of measurement: Apgar. | — |
Secondary
| Measure | Time frame |
|---|---|
| Adverse Effects. Timepoint: 1, 2, 4, 8 and 10 days after intervention. Method of measurement: Adverse drug effects form. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactRoya Kokabi
Fasa University of Medical Sciences
Outcome results
None listed