MedPath

Treatment of cutaneous leishmaniasis with thymol loaded chitosan gel

Phase 2
Recruiting
Conditions
Cutaneous leishmaniasis.
Cutaneous leishmaniasis
B55.1
Registration Number
IRCT20180526039848N1
Lead Sponsor
Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
50
Inclusion Criteria

There are at least two lesions, in one case intervention + glucantime and in the other lesion only glucantime is prescribed.
15 to 60 years
Skin lesions at least one centimeter in size
Leishmaniasis confirmed by a parasitologist
consent signature

Exclusion Criteria

People who do not use the drug according to the plan
People who do not go to the clinic on the scheduled days

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Measuring the lesion diameter (millimeters) using image processing software. Timepoint: From the first week of treatment and patient visit the clinic for the first time (once every three days to 45 days). Method of measurement: processing software.
Secondary Outcome Measures
NameTimeMethod
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