The effect of two topical drugs fluorouracil 5% and niacin amide 1% in the treatment of patients with actinic keratosis
Phase 2
Recruiting
- Conditions
- Actinic keratosis.Actinic keratosisL57.0
- Registration Number
- IRCT20220519054920N1
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 88
Inclusion Criteria
New patients with actinic keratosis who have not yet received any medication
Patients who have previously received topical medication and have not received topical medication in at least one month
People aged 18 and over
Non-hyperkeratotic lesions
Exclusion Criteria
Existence of other skin diseases at the treatment site
History of hypersensitivity to fluorouracil or niacin acid
Pregnant and lactating women
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Improvment rate. Timepoint: Before and after intervention. Method of measurement: Scoring based on the opinion of two dermatologists.;Dermoscopic grading. Timepoint: Before and after intervention. Method of measurement: Based on scoring by two dermatologist.;Complications of treatment. Timepoint: Weeks 4 and 8 in the fluorouracil group and weeks 6 and 12 in the niacinamid group. Method of measurement: Asking the patients.
- Secondary Outcome Measures
Name Time Method