MedPath

Comparison of the effects of vaginal estradiol and evening primrose pills in improving the visualization of the cervix during colposcopy

Phase 3
Recruiting
Conditions
Cesarean.
Encounter for cesarean delivery without indication
Registration Number
IRCT20140820018866N10
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
134
Inclusion Criteria

Women who are candidates for colposcopy and have an unsatisfactory colposcopy

Exclusion Criteria

Cervical structural anomalies such as history of cervical insufficiency, Müllerian anomaly and history of conization
Having contraindications or sensitivity to evening primrose or estradiol
Cancer in the patient or a history of breast or ovarian cancer in the family
History of smoking
Active vaginal bleeding or pregnancy
Post-menopausal women with an inflammatory pap smear or persistent vaginal discharge
Taking aspirin or Flavix
History of cardiovascular diseases and thromboembolism, sexually transmitted diseases, digestive diseases and neurological diseases, hypertension and coagulopathy, liver disease
Thyroid dysfunction and thyroid medication use
Blood disorders

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Satisfactoryness of colposcopy. Timepoint: 4 weeks after the start of drug administration. Method of measurement: colposcopy.
Secondary Outcome Measures
NameTimeMethod
Side effects such as stomach pain, breast pain, bloating, headache, itching, nausea and vomiting, diarrhea, chest or leg pain, impaired vision or speech, skin sensitivity, abnormal vaginal bleeding, vaginal itching and irritation. Timepoint: 4 weeks after the start of drug administration. Method of measurement: Ask the patient.
© Copyright 2025. All Rights Reserved by MedPath