CTRI/2022/12/048431
Not yet recruiting
未知
A single blinded, randomized controlled trial comparing the efficacy and safety of 1% Luliconazole cream plus 1% CiclopiroxOlamine cream, 1% Luliconazole cream plus 0.25% Amorolfine cream and 1% Luliconazole cream alone in the treatment of Tinea Corporis and Tinea cruris.
SRM Medical College Hospital & Research Centre, SRMIST, Potheri0 sites0 target enrollmentTBD
ConditionsHealth Condition 1: B354- Tinea corporis
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: B354- Tinea corporis
- Sponsor
- SRM Medical College Hospital & Research Centre, SRMIST, Potheri
- Status
- Not yet recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Patients of age 18years to 60 years, attending dermatology OPD of our hospital, and diagnosed to have Tinea corporis/cruris
- •2\. Positive KOH mount test from skin scraping
- •3\. Patients With mild to moderate extent of disease (less than 10% BSA involvement) and who are suitable for topical\-only antifungal therapy.
Exclusion Criteria
- •1\.Patients with known allergy to azole antifungals, Amorolfine or Ciclopiroxolamine.
- •2\.Pregnancy/ lactation
- •3\.Patients with dermatophytosis affecting nails / scalp/ palms / soles
- •4\.Patients with clinical features suggestive of secondary bacterial infections
- •5\.Patients on immunosuppressive therapy
- •6\.Patients who had used any topical medications for the tinea corporis/cruris lesions, in the last 2 weeks, or any systemic antifungal medications in the last 1 month.
- •7\.Patients who are not willing to participate in the study.
Outcomes
Primary Outcomes
Not specified
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