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Randomised, double-blind, parallel-group, comparative study of two terbinafine products

Conditions
tinea pedis (interdigital, Athlet´s foot)
Registration Number
EUCTR2008-007067-16-CZ
Lead Sponsor
JELFA SA
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

•clinical diagnosis of tinea pedis confirmed by microscopy and culture; detection of fungal hyphae
•age 18 +

Are the trial subjects under 18?
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

•prior radiotherapy or immunosuppressive therapy
•antimicrobial therapy within 2 weeks
•the presence of systemic fungal disease
•chronic plantar tinea pedis
•the presence of bacterial infection
•application of topical antifungals within 28 days
•concurrent onychomycosis
•pregnancy and breasfeeding

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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