Induction and Promotion of labor. Spontaneous vertex deliveryr
Conditions
Interventions
Intervention 1: Intervention group oxytocin alone with dose 2 mIU/min which increase every 15 min. Intervention 2: Intervention group oxytocin plus intravenous propranolol, oxytocin with dose 2 mIU/mi
Treatment - Drugs
Intervention group oxytocin alone with dose 2 mIU/min which increase every 15 min
Intervention group oxytocin plus intravenous propranolol, oxytocin with dose 2 mIU/min which increase every 15 min and propranolol 2 mg/ml IV
Intervention group oxytocin plus oral propranolol, oxytocin with dose 2 mIU/min which increase every 15 min and propranolol 20 mg oraly
Sponsors
Vice Chancellor for Research of Kurdistan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: Inclusion Criteria: Nulliparity, singleton, cephalic presentation, fetal heart rate between 120 to 160 beats per minute, approximate weight of 2,500 to 4,000 (by examination or ultrasound), the maternal heart rate between 60 to 130 beats per minutes. Exclusion Criteria: CPD, any history of previous surgery on the uterus, fetal distress, the risk of macrosomia or polyhydramnius, SBP=100, PR=60, PR=130 min, any history of cardiopulmonary disease, metabolic disease of mother or taking medicine for any illness by mother.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The duration of phases of labor. Timepoint: From the intervention to delivery. Method of measurement: vaginal exam. | — |
Secondary
| Measure | Time frame |
|---|---|
| Pregnancy ending in caesarean section. Timepoint: After the second period of injection. Method of measurement: Based on the indications for cesarean section. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Narjes Marjani
Kurdistan University of Medical Sciences
Outcome results
None listed