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Comparison of the effect of vaginal consumption of primrose oil on the preparation of cervix in term delivery at patient resort to educational hospitals of Medical Sciences

Early Phase 1
Recruiting
Conditions
Pregnant mothers.
Newborn (suspected to be) affected by other specified complications of labor and delivery
P03.8
Registration Number
IRCT20201115049389N1
Lead Sponsor
Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
76
Inclusion Criteria

Low risk of pregnancy
Bishop score less than 4
BMI between 19 and 25
Lack of systemic disease
No drug addiction
No vaginal bleeding
Gain conscious satisfaction

Exclusion Criteria

Patient non-cooperation
Increased risks of delivery
Use other methods of uterine preparation
Diabetes and hypertension
Chronic inflammatory disease
Improper fetal presentation

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Bishop score measured. Timepoint: Before interventional and 24 hours after intervention. Method of measurement: questionnaire.
Secondary Outcome Measures
NameTimeMethod
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