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Compare the effectiveness of Tablet Fluconazole, Capsule Itraconazole and Tablet Terbinafine in superficial fungal infections

Randomised control trial to study the effectiveness of Tablet Fluconazole, Capsule Itraconazole and Tablet Terbinafine in Superficial Dermatophytosis - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/061561
Enrollment
180
Registered
2024-01-18
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: B354- Tinea corporis

Interventions

Intervention1: Randomised control trial to study the effectiveness of Tablet Fluconazole, Capsule Itraconazole and Tablet Terbinafine in Superficial Dermatophytosis: Patients will be randomly allocate

Sponsors

Command Hospital Airforce Bangalore
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients with tinea corporis, tinea cruris, tinea pedis or tinea faciei or any combination of these conditions will be included in the trial 2.Age more than 18 years 3.Both male and female 4.Plaque of more than or equal to 4 in one anatomical site or plaque in two different anatomical sites 5.Free of any antifungal treatment for the previous 28 days 6.Direct microscopy with KOH positive for fungal elements 7.Patients giving consent 8.Chronic or chronic relapsing tinea, duration of tinea more than or equal to 3 months, or tinea present for more than or equal to 3 months that improved within this period but relapsed within a month

Exclusion criteria

Exclusion criteria: 1.Liver disorders 2.Renal disorders 3.Cardiovascular abnormalities 4.Allergic to azoles and allylamines 5.Pregnancy and lactation 6.Tinea manuum, tinea unguium • Immunosuppressive patients and on Immunosuppressive drugs • History of drug reaction or allergy to any of the three drugs • Inability to attend follow-up every 2 weeks • Abnormal results in complete blood count (CBC), liver function test (LFT), renal function test (RFT), abnormal blood sugar levels

Design outcomes

Primary

MeasureTime frame
To determine the most effective antifungal drug for the treatment of superficial dermatophytosisTimepoint: one & half year

Secondary

MeasureTime frame
1.To assess the safety profile and time take for clinical cureTimepoint: One and half year;2.To compare the efficacy of these three oral antifungal drugsTimepoint: One and half year

Countries

India

Contacts

Public ContactDr Arun Kumar Singh

Command Hospital Airforce Bangalore

debdeep5000@gmail.com8811851830

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026