Ripening cervix.
Conditions
Interventions
Intervention 1: First intervention group: In the dual drug group, misoprostol is given at a dose of 25 micro grams vaginal with nitroglycerin 40 mg vaginal and after 6 hours, the cervix is examined f
Sponsors
Qazvin University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Primigravida Gestational age>=37 week Bishop score5 Singleton
Exclusion criteria
Exclusion criteria: Surgery on the uteus or previous cesarean section chronic hypertension and preeclampsia uterine contractions The presence of heart, kidney and liver disease rapture of membrane IUGR Suspected embryonic anomalies chorioamnionitis Fever above 38 ° C polyhydramnios Pre-delivery hemorrhage fetal distress
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The duration of cervical ripening until delivery. Timepoint: 6 and 12 hours. Method of measurement: Vaginal exam. | — |
Secondary
| Measure | Time frame |
|---|---|
| Duration of taking the drug until the onset of the active phase of labor. Timepoint: every 2 hours. Method of measurement: Vaginal exam.;Duration of taking drug until delivery. Timepoint: every 2 hours. Method of measurement: Vaginal exam.;Duration of the fist phase of labor. Timepoint: every 2 hours. Method of measurement: Vaginal exam.;Duration of the second phase of labor. Timepoint: every 1 hours. Method of measurement: Vaginal exam.;Reach to vaginal delivery. Timepoint: After delivery. Method of measurement: Date sheet.;Type of delivery. Timepoint: After delivery. Method of measurement: Date sheet. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMaryam Rafiee
Qazvin University of Medical Sciences
Outcome results
None listed