Comparison of the effect of intralesional injection of triamcinolone acetonide with the simultaneous combination of triamcinolone acetonide and 5-fluoracil
Not Applicable
Recruiting
- Conditions
- Hypertrophic scar.
- Registration Number
- IRCT20130812014333N189
- Lead Sponsor
- Kermanshah University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Informed consent
Exclusion Criteria
Patients under treatment for the last 6 months
Pregnant patients or those planning to become pregnant
Lactating women
Chronic kidney disease patients or those with any abnormal changes in CBC or liver function tests
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intensity of itching of the lesion. Timepoint: First, fourth and sixth week. Method of measurement: Based on examination and questioning of the patient.;Redness intensity of the lesion. Timepoint: First, fourth and sixth week. Method of measurement: Based on examination.;Length, width and height of the lesion. Timepoint: First, fourth and sixth week. Method of measurement: Based on examination.
- Secondary Outcome Measures
Name Time Method