induction of labour.
Conditions
Interventions
Intervention 1: Intervention group: Recipient of 50 µg misoprostol by buccal method up to three doses in case of no onset of labor pain. Intervention 2: Intervention group: Recipient of 50 µg misopros
Sponsors
Qazvin University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: single, bishop score=4, cephalic presentation, NST reactive, parity =2, gestational age more than 37 w, Amniotic fluid index =5
Exclusion criteria
Exclusion criteria: maternal medical diseases breech presentation fetal anomaly
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| The rate of Cesarean section. Timepoint: delivery. Method of measurement: cesarean/ NVD.;Reason of cesarean. Timepoint: during delivery. Method of measurement: mecunium, FHR deceleration, No responce to induction.;Time to the active phase of labor. Timepoint: 0-6-24 hr. Method of measurement: Bishop Score.;Need for oxytocin. Timepoint: until delivery. Method of measurement: yes/no.;Number of misoprostol doses. Timepoint: until delivery. Method of measurement: 1-2-3.;Fetal complications. Timepoint: until delivery. Method of measurement: abnormal pattern of fetal heart rate, meconium, Apgar score 1 and 5 postpartum, and admission to neonatal intensive care unit.;Maternal complication. Timepoint: until delivery. Method of measurement: Fever, chills, nausea, vomiting, uterine tachysystole, uterine hyperstimulation. | — |
Primary
| Measure | Time frame |
|---|---|
| The effect of misoprostol in induction of labor. Timepoint: every 6h to 24h. Method of measurement: bishop score and time of delivery. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactRazieh Akbari
Qazvin University of Medical Sciences
Outcome results
None listed