RecruitingPhase 4NCT07342153

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


Sponsor

Urooj Fatima

Enrollment

126 participants

Start Date

Nov 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

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 oral antifungal drugs - fluconazole and itraconazole - in people with resistant tinea corporis. Adults aged 18-70 years who have had persistent disease for at least six months will be enrolled at the Dermatology Department of CDA Hospital, Islamabad. Participants will be randomly assigned to one of two groups. One group will receive itraconazole 200 mg once daily for four weeks, and the other group will receive fluconazole 150 mg every other day for four weeks. Neither group will know which medicine they are receiving (blinded allocation). The main goal is to find out which medicine works better in achieving complete clinical resolution - meaning no redness, no scaling, no itching, and no visible skin lesions - after four weeks of treatment. Doctors will measure the severity of symptoms using a standard scoring system, and patients will also report their level of itching. The findings will help guide doctors in Pakistan and similar regions in choosing the most effective oral antifungal for patients with resistant tinea corporis, improving both treatment success and patient quality of life.


Eligibility

Min Age: 18 YearsMax Age: 70 Years

Inclusion Criteria4

  • 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 Criteria5

  • Prior use of oral antifungal therapy within the past 3 months
  • Recent antibiotic treatment for superadded bacterial skin infection in the past 1 month
  • Known immunosuppressive conditions (e.g., diabetes mellitus, malignancy)
  • Current or recent use of immunosuppressive drugs
  • Pregnant or lactating women

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGItraconazole (200 mg)

Oral itraconazole 200 mg once daily for 4 weeks. Assigned to participants in the Itraconazole Group. FDA-approved antifungal drug being evaluated for comparative effectiveness in resistant tinea corporis.

DRUGFluconazole 150 mg

Oral fluconazole 150 mg every other day for 4 weeks. Assigned to participants in the Fluconazole Group. FDA-approved antifungal drug being evaluated for comparative effectiveness in resistant tinea corporis.


Locations(1)

CDA Hospital Islamabad

Islamabad, Punjab Province, Pakistan

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07342153


Related Trials