comparison of the effectiveness of 5-FU and tacrolimus ointment in the treatment of vitiligo vulgaris
Phase 2
Recruiting
- Conditions
- vitiligo vulgaris.Vitiligo
- Registration Number
- IRCT20230115057128N1
- Lead Sponsor
- Ilam University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
The presence of at least two vitiligo lesions in the upper, lower and trunk limbs similar in size and color (if the patient had several depigmented lesions, among them two lesions that were similar in size and color were selected would be)
Age above 12 years
have the possibility to refer and follow up
Consent based on participating in the study
Not using topical treatments in the last month
The steady or progressive course of the disease in a person
Occupancy of at least 10% of the body surface by this disease
Not having an immune deficiency
Exclusion Criteria
Patients with skin lesions on the face
Cases of segmental vitiligo
pregnancy
Inability to track treatment results
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Size of the lesion. Timepoint: Examining the lesions at the beginning of the study and the second, fourth and sixth months after the start of treatment. Method of measurement: VASI scoring system.;Percentage of pigmentation. Timepoint: Examining the lesions at the beginning of the study and the second, fourth and sixth months after the start of treatment. Method of measurement: VASI scoring system.
- Secondary Outcome Measures
Name Time Method