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Efficacy Of Topical Terbinafine And Sertaconazole In Combination With Oral Itraconazole In Treatment Of Dermatophytosis

To Study The Efficacy Of Oral Itraconazole 200mg OD with Topical 1% Terbinafine Cream Versus Oral Itraconazole 200mg OD With Topical 2% Sertaconazole Cream In Dermatophytosis: A Within Person Pilot Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/08/027328
Enrollment
50
Registered
2020-08-24
Start date
Unknown
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Health Condition 1: L088- Other specified local infections of the skin and subcutaneous tissue

Interventions

Intervention1: Oral itraconazole with topical sertaconazole: Two comparable tinea lesions (size, location and symmetry) with less than or equal to one cm variation in size will be selected in each pat

Sponsors

Armed Forces Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adults between the age of 18-65 years, clinically diagnosed as tinea corporis and tinea cruris and confirmed by positive KOH mount microscopy

Exclusion criteria

Exclusion criteria: Anyone who has taken systemic or topical antifungals in the four weeks prior to initiation of study; or presents with solitary lesion, history of hypersensitivity to antifungals, on any systemic medications known to have interactions with itraconazole, or with superadded bacterial infections, pregnancy or lactating and on immunosuppressive drugs or with any immunosuppressive disease.

Design outcomes

Primary

MeasureTime frame
Complete cure: Clearance on microscopy, no residual signs & symptoms (Except Post inflammatory hyperpigmentation) Mild resolution: Upto 25% improvement Moderate resolution: 25-50% improvement Significant resolution: 51-99% improvementTimepoint: 0, 2 and 4 weeks

Secondary

MeasureTime frame
Side effects due to the medicationsTimepoint: 0, 2 and 4 weeks;Time of clinical cure and improvementTimepoint: 0, 2 and 4 weeks

Countries

India

Contacts

Public ContactLt Col Dr Ruby Venugopal

Armed Forces Medical College, Pune, Maharashtra

ruby4972@gmail.com7837766357

Outcome results

None listed

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