A comparative study of misoprostol and evening primrose for cervical ripening before gynecologic procedures

Not Applicable

• Conditions: gynecologic.; Encounter for gynecological examination; Z01.4

• Registration Number: IRCT20151228025732N50
• Lead Sponsor: Semnan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 30 May 2022

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 40

Inclusion Criteria

Women 25 to 75 years old
Candidate for gynecology surgery

Exclusion Criteria

Heart disease, Liver, Asthma, Seizure
Infection
Bleeding Disorders
Taking anticoagulants

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The rate of cervical opening. Timepoint: Before and after intervention. Method of measurement: Sonography.