Comparing the Efficacy of Oral Fluconazole Versus Oral Itraconazole in Treating Resistant Tinea Corporis

Recruiting Phase 4 Interventional Study
Tinea Corporis Dermatophytosis
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 70
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Treatment
Participants needed
126 (estimated)
Sponsor
Urooj Fatima · Other
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About This Trial
Tinea corporis (commonly called "ringworm of the body") is a skin infection caused by fungi that often becomes difficult to treat when it persists despite creams or other medicines. In recent years, many patients have developed infections that do not respond to routine antifungal treatments, which causes long-term itching, redness, and scaling of the skin. This study will test two commonly used o…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: Adults aged 18-70 years Male or female Clinical diagnosis of resistant tinea corporis, defined as persistent disease ≥6 months despite topical antifungal therapy Microscopic confirmation of fungal hyphae on KOH preparation of skin scrapings Exclusion Criteria: Prior use of …
Contacts

Urooj Fatima, MBBS

+923363005069

urooj29scorpio@gmail.com

CONTACT