Efficacy of combined topical treatment versus cryotherapy for the treatment of refractory warts
Phase 3
Recruiting
- Conditions
- Hand and foot wart.Plantar wartB07.0
- Registration Number
- IRCT20221109056452N1
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
Treatment-resistant warts
Consent to participate in the study
Exclusion Criteria
Pregnant and lactating women
Children under four years old
People over 65 years old
Patients under immunosuppressive treatment
Patients with immunodeficiency and hypersensitivity reactions
Patients with vascular diseases
Patients with Raynaud's phenomenon
Patients with capillary filling more than two seconds
Patients with rheumatological disorders
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Effectiveness of treatment according to the physician. Timepoint: 4 and 8 weeks after intervention. Method of measurement: Physician global assessment.;Effectiveness of treatment according to the patient. Timepoint: 4 and 8 weeks after intervention. Method of measurement: Patient global assessment.;Local pain. Timepoint: 4 and 8 weeks after intervention. Method of measurement: Visual analogue scale.
- Secondary Outcome Measures
Name Time Method