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Comparison the effect of oral propranolol and oxytocin with oxytocin alone on duration of labor and type of delivery in nulliparous women with prolonged pregnancy.

Comparison the effect of oral propranolol and oxytocin with oxytocin alone on duration of labor and type of delivery in nulliparous women with prolonged pregnancy.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201105316575N3
Enrollment
146
Registered
2011-07-23
Start date
2008-09-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

The effect of oral propranolol on the duration of labor and type of delivery in nulliparous women with prolonged pregnancy.. Prolonged pregnancy

Interventions

Intervention 1: The first group: induction was performed with low dose method. Intervention 2: The second group: 20 mg propranolol was administered orally then induction was performed based low dose m
Treatment - Drugs
The first group: induction was performed with low dose method
The second group: 20 mg propranolol was administered orally then induction was performed based low dose method. Orally propranolol(20 mg) was administered every 8 hours during the induction

Sponsors

Vice chancellor for research, Ilam University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:35-18 years of age; primiparous; singleton pregnancy; gestational age40-42; without CPD; Bishop score less than 5; optimal care during pregnancy; blood pressure less than 140/90 mmHg; pulse 60-110; body mass index 19/8-26(kg/m) before pregnancy; intact of membran; estimated fetal weight less than 4000 grams; Excluding criteria: Polyhydramnios; abnormal presentation; preeclampsia; known medical conditions before and during pregnancy such as asthma; cardiovascular and metabolicat disease at the admission time

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Duration of labor in nulliparus women with prolonged pregnancy. Timepoint: Start of admission in hospital to 24h after delivery. Method of measurement: Duration of labor according to minute.

Secondary

MeasureTime frame
Type of delivery. Timepoint: Start of admission in hospital to 24h after delivery. Method of measurement: Type of delivery vaginal or cesarean.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAshraf Direkvand-Moghadam

Department of Midwifery, Ilam University of Medical Sciences

direkvand-a@medilam.ac.ir+98 918 342 0061

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026