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Comparing effect of oxytocin versus oxytocin-propranolol combination on labor progressio

Phase 2
Conditions
]nduction and Promotion of labor.
Spontaneous vertex delivery
Registration Number
IRCT2016092629983N1
Lead Sponsor
Gorgan Congenital malformations research center, Golestan University of Medical Sciences,Gorgan, Ira
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
130
Inclusion Criteria

37 to 41 weeks gestational age based on reliable LMP and ultrasound confirmation in the first quarter, also nuliparity; singleton, cephalic presentation;, intact membranes , bishop score equal to or less than 5.
Exclusion criteria: CPD; any history of previous surgery on the uterus; fetal distress; the risk of macrosomia or polyhydramnius; SBP=100; PR=60; PR=120 min; any history of cardiopulmonary disease; known metabolic disease of mother or taking medicine for any illness in the mother.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The duration of phases of labor. Timepoint: Since the intervention untile delivery. Method of measurement: vaginal exam.
Secondary Outcome Measures
NameTimeMethod
eonate s Apgar. Timepoint: After Delivery. Method of measurement: According to the protocol.;Pregnancy ending in caesarean section. Timepoint: After the second period of injection. Method of measurement: Based on the indications for cesarean section.
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