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Comparison of oral misoprostol and Intravenous oxytocin for induction of labor at Premature rupture of membrane in primigravida wome

Not Applicable
Conditions
Pregnancy, childbirth and the puerperium.
Other complications of anaesthesia during labour and delivery
Registration Number
IRCT201104131946N9
Lead Sponsor
Vice chancellor for researchr, Guilan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Male
Target Recruitment
240
Inclusion Criteria

a) single pregnancy (between 36 to 42 weeks); b)vertex presentation; c)bishop score equal or less than four; d) absence of uterus spontaneous contractions;e)normal fetal heart rate; f) cephalopelvic proportion. Exclusion criteria: a) sensitivity to PGs; b) previous history of cesarean; c) uterus wall scar; d) preeclampsia or blood pressure more than 140/90 mmHg; e) history of heart disease ,asthma, glaucoma; f)IUGR; g)age under18 years

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Comparison of oral misoprostol and Intravenous oxytocin. Timepoint: Every four hours up to two times. Method of measurement: Vaginal examination and record in Questionnaire.
Secondary Outcome Measures
NameTimeMethod
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