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Comparison of the effect of misoprostol and propranolol with misoprostol alone in induction of labor

Phase 3
Conditions
Induction of labor.
Failed induction of labor
Registration Number
IRCT20230125057217N1
Lead Sponsor
Qazvin University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Female
Target Recruitment
240
Inclusion Criteria

Gestational age between 38 and 42 weeks
Singleton
Cephalic presentation
Bishop score less than 5

Exclusion Criteria

Uterine contractions
History of caesarean section
Fetal distress
Rupture of membran
Macrosomy
Systolic blood pressure below 100 mm Hg and pulse below 60 and above 120

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Duration of labor. Timepoint: End of study. Method of measurement: Based on the time measured from induction of labor to final delivery.;Apgar score. Timepoint: 1 and 5 minutes after birth. Method of measurement: Examination.;The duration of the first phase of labor. Timepoint: After delivery. Method of measurement: Information entered in the patient's delivery record.;The duration of the second phase of labor. Timepoint: After delivery. Method of measurement: Information entered in the patient's delivery record.;The duration of the latent phase of labor. Timepoint: After delivery. Method of measurement: Information entered in the patient's delivery record.;Postpartum bleeding. Timepoint: One hour after delivery. Method of measurement: Estimate the amount of bleeding by the delivery agent to cc.
Secondary Outcome Measures
NameTimeMethod
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