MedPath

Topical treatment of cutaneous leishmaniasis with lipozomal azithromyci

Phase 2
Conditions
Cutaneous Leishmaniasis.
Cutaneous Leishmaniasis
Registration Number
IRCT2014031216955N1
Lead Sponsor
Mashhad University of Medical Sciences, Vice Chancellor for Research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
66
Inclusion Criteria

Presence of cutaneous leishmaniasis with less than 12 weeks of clinical course; Not receive any treatment before
Exclusion criteria: Pregnancy; Lactating; Receiving simultanous treatment with other methods during treatment course; Sensitivity or intolerance to Macrolids;
History of significance renal; Pulmonary and cardiovascular disease

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
esion improvement. Timepoint: Weekly until 6 weeks. Method of measurement: Measuring the size of induration and ulcer by caliper.
Secondary Outcome Measures
NameTimeMethod
Side effects. Timepoint: Weekly. Method of measurement: Clinical evaluation.
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