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To study the result and safety of 2 different antifungal medicines in ringworm infection of skin.

To study the efficacy and safety of Conventional Itraconazole vs Super bioavailable Itraconazole in dermatophytic infections. - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/069557
Enrollment
108
Registered
2024-06-26
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Health Condition 1: B359- Dermatophytosis, unspecified

Interventions

Intervention1: Super Bioavailable Itraconazole: Super Bioavailable Itraconazole at a dose of 50 mg twice daily given orally for a duration of 4 to 6 weeks in case of dermatophytic infections with regu

Sponsors

AIIMS Hospital Raebareli
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ALL patients with dermatophytic infections except fungal infections of hair and nail Body surface area >20% positive koh mount

Exclusion criteria

Exclusion criteria: Pregnant and lactating females pts with liver dysfunction Pt already taken any other antifungal drug/ steroids ( apart from topical agents) 2 weeks prior Children Pts with congestive heat failure and pts who develop hypersensitivity reaction to itraconazole or any of its component

Design outcomes

Primary

MeasureTime frame
Complete cure achieved at the end of 4 weeks or at the end of 6 weeks decided by both: CLINICAL CRITERIA: Relief in itching Healing of plaques Healthy normal skin LABORATORICAL CRITERIA: Negative KOH mount for fungal infectionTimepoint: 4 WEEKS 6 WEEKS

Secondary

MeasureTime frame
Any other adverse effects experienced by patientTimepoint: 4 WEEKS 6 WEEKS;Safety of Conventional Itraconazole vs Super Bioavailable Itraconazole tested by: Liver Function Tests at 4th & 6th week. Timepoint: 4 WEEKS 6 WEEKS

Countries

India

Contacts

Public ContactDr SAKSHI

AIIMS Raebareli

dramritaupadhyaya@gmail.com9899985028

Outcome results

None listed

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