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Therapeutic effect of TCA on anogenital warts

Phase 2
Conditions
Anogenital wart.
Anogenital (venereal) warts
Registration Number
IRCT201307153566N3
Lead Sponsor
Tabriz University of Medical Sciences, assistance research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
100
Inclusion Criteria

patients with anogenital warts that their disease was detected by the clinical or pathological evidence.
Exclusion criteria: patient with anogenital pathological defect and pregnancy.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
umber of warts. Timepoint: The patients for eleven months and at weeks zero, one, two, three, and four, two months later, three months later, fiv months later e, seven months later, nine months later and eleven months later of treatment follow up. Method of measurement: Physical exam.
Secondary Outcome Measures
NameTimeMethod
Skin irritation. Timepoint: The patients for eleven months and at weeks zero, one, two, three, and four, two months later, three months later, fiv months later e, seven months later, nine months later and eleven months later of treatment follow up. Method of measurement: Physical exam.;Itching. Timepoint: The patients for eleven months and at weeks zero, one, two, three, and four, two months later, three months later, fiv months later e, seven months later, nine months later and eleven months later of treatment follow up. Method of measurement: Physical exam.;Fever. Timepoint: The patients for eleven months and at weeks zero, one, two, three, and four, two months later, three months later, fiv months later e, seven months later, nine months later and eleven months later of treatment follow up. Method of measurement: Physical exam.
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