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Study of skin features, laboratory features and response to treatment to antifungal drugs in patients with superficial fungal infections.

A Clinico-Mycological, Therapeutic and Antifungal drug sensitivity study of Extensive dermatophytosis.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/04/013045
Enrollment
150
Registered
2018-04-04
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- EXTENSIVE DERMATOPHYTIC INFECTIONS

Interventions

Intervention1: ITRACONAZOLE: Group A - systemic Itraconazole 5 mg/kg body weight (BW) once daily for a period of 6 weeks. Control Intervention1: GRISEOFULVIN: Group B â?? Griseofulvin 10 mg/kg Body we

Sponsors

MAHARAJAHS INSTITUTE OF MEDICAL SCIENCES
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Clinically diagnosed cases of extensivedermatophytoses infection affecting more than one region of the body. 2. Both sexes between the age groups 18 - 70 yrs 3.Patients who have not used topical and systemic antifungal drugs for the past 6 weeks.

Exclusion criteria

Exclusion criteria: 1.Infants, below 18 yrs, above 70 yrs 2.Immunocompromised patients including HIV are excluded. 3.Pregnancy and lactating patients are excludued. 4.Patients receiving multiple drugs for medical conditions including glucocorticosteroids.

Design outcomes

Primary

MeasureTime frame
1.Cinical profile of dermatophytic infections prevalent in this region will be noted. 2. Mycological profile of dermatophytic infections including species identification prevalent in this region will be noted. 3. Sensitivity pattern of isolates against terbinafine, itraconazole,griseofulvin will be studied and recorded. 4. Therapeutic efficacy of single and in combinations of systemic antifungal drugs in extensive dermatophytic infections will be reported. Timepoint: 8 weeks

Secondary

MeasureTime frame
1. To note the recurrences in the follow up period of 6 months.Timepoint: 6 months

Countries

India

Contacts

Public ContactVanapalli Ramani Sneha

Maharajahs Institute Of Medical Sciences

tnr_derma@yahoo.com9849129912

Outcome results

None listed

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