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Comparison of the effects of sublingual Misoprostol and Oxytocy

Not Applicable
Conditions
abor.
Single spontaneous delivery
Registration Number
IRCT2013032512856N1
Lead Sponsor
Hamedan University of Medical Sciences, research department
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
82
Inclusion Criteria

singleton pregnancy; first or second alive delivery; Bishop Score of 4 or more, no history of any internal disorders, age between 18 to 35 years old.
Exclusion criteria: twin pregnancy and contraindications of induction.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
abor time. Timepoint: Before and after intervention. Method of measurement: Hour.
Secondary Outcome Measures
NameTimeMethod
Time to Bishop 8 and kind of delivery. Timepoint: After intervention. Method of measurement: Questionnaire.
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