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Imiquimod therapy after surgical removal of anal HPV-lesions to reduce likelihood of recurrence

Phase 1
Conditions
anal HPV-lesions
Therapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Therapeutic techniques [E02]
Registration Number
EUCTR2017-000842-23-AT
Lead Sponsor
Medical University Innsbruck
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
200
Inclusion Criteria

- age >=18 years
- Indication of surgical sanitation of HPV-lesions in anal area by means of fulguration

Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 150
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 50

Exclusion Criteria

- participation in other trials
- diagnosis of HPV-associated lesions in the last 12 month
- known allergy to Imiquimod
- pregnant of lactating women

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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