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Tranxamic acid in cervical ectropio

Phase 3
Conditions
Cervical ectropion.
Erosion and ectropion of cervix uteri
Registration Number
IRCT20220115053719N1
Lead Sponsor
Zanjan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Female
Target Recruitment
88
Inclusion Criteria

Patients who have been diagnosed with cervical ectropion by an experienced gynecologist.

Exclusion Criteria

Pregnancy
Having any known malignancy
Patients in the Menopause period
Intrauterine device (IUD)
Taking contraceptives in the recent 3 months

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pelvic pain. Timepoint: Patients' pain will be evaluated at intervals of zero, the seventh day, the fourteenth day, the twenty-first day, the twenty-eighth day, the sixtieth day and the ninetieth day. Method of measurement: Visual Analogue Scale will be used to determine the pain.
Secondary Outcome Measures
NameTimeMethod
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