duration of labor. long labour
Conditions
Interventions
Intervention 1: 2 mg propranolol before oxytocin ( intervention group ). Intervention 2: normal saline as placebo before oxytocin ( control group ).
Treatment - Drugs
2 mg propranolol before oxytocin ( intervention group )
normal saline as placebo before oxytocin ( control group )
Sponsors
Shahid Beheshti University of Medical Science
Eligibility
Sex/Gender
Female
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: GA>34 w; singleton pregnancy; cephalic presentation; no contraindication of vaginal delivery;cervical dilatation 60 per minutes; no history of uterine scar; patient inform consent. Exclusion criteria: lack of consent at every stage of research.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Duration of labor. Timepoint: from induction of labor to delivery. Method of measurement: minutes. | — |
Secondary
| Measure | Time frame |
|---|---|
| Cesarean rate. Timepoint: at the last of study. Method of measurement: hospital documents.;Neonatal Apgar. Timepoint: first and fifth minutes. Method of measurement: Apgar score.;Fetal complications. Timepoint: at the last of study. Method of measurement: physical exam.;Maternal complications. Timepoint: at the last of study. Method of measurement: history - physical exam.;Oxytocin dosage. Timepoint: at the last of study. Method of measurement: hospital documents. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactLeila Nazari
Shahid Beheshti University of Medical Science
Outcome results
None listed