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Effectiveness of 5% fluorouracil ointment in the treatment of genital warts

Phase 2
Recruiting
Conditions
Genital wart.
Viral warts
Registration Number
IRCT20230913059421N1
Lead Sponsor
Ahvaz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

Patients who are diagnosed with genital warts for the first time or who have not received treatment for genital warts in the last three months.
Do not have any other skin disease

Exclusion Criteria

Patients with immune system dysfunction
Having a previous history of allergy to the studied drugs
Pregnant and lactating women

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ocation of the lesion. Timepoint: Before treatment, 1 and 3 months after treatment. Method of measurement: Physical examination.;The size of the lesion. Timepoint: Before treatment, 1 and 3 months after treatment. Method of measurement: Physical examination.;Number of genital warts. Timepoint: Before treatment, 1 and 3 months after treatment. Method of measurement: Physical examination.
Secondary Outcome Measures
NameTimeMethod
Recurrence of the disease. Timepoint: Before treatment, 1 and 3 months after treatment. Method of measurement: Physical examination.;Side effects. Timepoint: 1 and 3 months after treatment. Method of measurement: Physical examination.
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