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Clofazimine Effect on Cutaneous Leishmaniasis

Not Applicable
Conditions
Cutaneous Leishmaniasis.
Cutaneous Leishmaniasis
Registration Number
IRCT138710251543N1
Lead Sponsor
Fars University of Medical Sciences and Health Services
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
24
Inclusion Criteria

Age more than 12 y/o, duration of disease less than 2month, no anti-leishmania (Glucantim, Rifampin, Azithromycin) treatment since 1 month prior to study,
Exclusion criteria: Lesion on face and joint, pregnancy, lactation, severe diseases including hepatic, renal and cardiac diseases

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Complete healing with re-epithelialization of cutaneous lesion. Timepoint: 3 week. Method of measurement: Physical examination and change of score, including: erythema, induration, ulceration and size of lesions.
Secondary Outcome Measures
NameTimeMethod
Adverse effect. Timepoint: 3 weeks. Method of measurement: Physical examination and medical history.
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