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

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20151228025732N50

Enrollment

Registered

2020-02-08

Start date

2020-03-01

Completion date

Unknown

Last updated

2022-05-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

gynecologic. Encounter for gynecological examination

Interventions

Intervention 1: Intervention group: According to the protocol, they will receive evening primrose (4 capsules) vaginally 2 hours before surgery. Intervention 2: Intervention group: According to the pr

Eligibility

Sex/Gender

Female

Age

25 Years to 75 Years

Inclusion criteria

Inclusion criteria: Women 25 to 75 years old Candidate for gynecology surgery

Exclusion criteria

Exclusion criteria: Heart disease, Liver, Asthma, Seizure Infection Bleeding Disorders Taking anticoagulants

Design outcomes

Primary

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

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNahid Rahbar

Semnan University of Medical Sciences

are20935@yahoo.com+98 23 3345 1336

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026