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Evaluation of the effect of castor oil and evening primrose on cervical ripening

Phase 3
Conditions
cervix ripening.
Registration Number
IRCT20160809029281N3
Lead Sponsor
Yazd University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
114
Inclusion Criteria

Iranian citizenship
Single twin
BiShop score below four4
Tend to have a normal delivery
a low-risk pregnancy (no diabetes, no preeclampsia, bleeding, etc.)
Age 18-35 years
Having h eight shorter than 150 cm
Water bag closed
Fetal weight according to sono2500-4000
No bleeding diseases
Head displayFetal health according to sono
Fetal health according to sono
No known or systemic chronic diseases in the mother

Exclusion Criteria

Use of any narcotics or herbal medicines
Any vaginal bleeding
Having a midwife with a private

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Cervical ripening. Timepoint: 40 weeks of pregnancy, 48 hours after intervention. Method of measurement: Determine the B-score score, which includes five characteristics: dilatation, effusion, fetal position, consistency, and cervical condition. The most common scoring system is to predict the success or failure of induction of labor.
Secondary Outcome Measures
NameTimeMethod
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