Comparison of efficacy and safety of topical 5% potassium hydroxide solution and topical 0.1% retinoid lotion in the treatment of plane wart
Not Applicable
- Conditions
- plane wart.Viral infections characterized by skin and mucous membrane lesionsB00-B09
- Registration Number
- IRCT201201038516N2
- Lead Sponsor
- The institute of research and technology of Ahvaz jundishapur University of Medical Science
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 72
Inclusion Criteria
Inclusion criterion: presence of at least three lesion
Exclusion criteria:
1-Pregnancy
2-Lactation
3-Patients that have received treatment in the recent four weeks
4-Secondary infection
5-Involvement of the genital area
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Improvement. Timepoint: 2 weeks, 4 weeks, 6 weeks after initiation of the treatment and 2 weeks after the end of the treatment. Method of measurement: Based on the count of lesions.
- Secondary Outcome Measures
Name Time Method Adverse drug reaction. Timepoint: 2 weeks, 4 weeks, 6 weeks after the initiation of the treatment and 2 weeks after the end of the treatment. Method of measurement: Based on occurrence of various adverse reaction.