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Effects of propranolol on labor

Not Applicable
Conditions
duration of labor.
long labour
Registration Number
IRCT201211108151N4
Lead Sponsor
Shahid Beheshti University of Medical Science
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
140
Inclusion Criteria

GA>34 w; singleton pregnancy; cephalic presentation; no contraindication of vaginal delivery;cervical dilatation < 3 cm; absence of active phase; no contraindication of propranolol; no history of maternal hearth disease , diabetes mellitus and lupus; maternal pulse rate > 60 per minutes; no history of uterine scar; patient inform consent. Exclusion criteria: lack of consent at every stage of research.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Duration of labor. Timepoint: from induction of labor to delivery. Method of measurement: minutes.
Secondary Outcome Measures
NameTimeMethod
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.
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