Evaluation of treatment of actinic keratosis with KOH5% solution in comparison to Fluorouracil 5% cream
Phase 3
- Conditions
- Actinic Keratosis.Actinic keratosis
- Registration Number
- IRCT20180909040978N1
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 25
Inclusion Criteria
Patients suffering Actinic Keratosis attending Razi dermotology hospital
Having at least 18 years of age
Having a minimum number of 8 lesions( 4 on each side, at least) on parts of skin that are exposed to the sun.
Exclusion Criteria
Pregnant women
People with a history of allergy to any of the drugs under study.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Smoothing of Actinic Keratosis's lesions' roughness. Timepoint: At the beginning of the study (Before the intervention begins) and 14, 28, 60 and 90 days after starting the use of KOH 5% solution and Fluorouracil cream. Method of measurement: Clinical diagnosis by dermatologist.
- Secondary Outcome Measures
Name Time Method