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eech treatment of Leishmaniasis lesio

Not Applicable
Recruiting
Conditions
Cutaneous leishmaniasis.
Cutaneous leishmaniasis
B55.1
Registration Number
IRCT20211211053349N3
Lead Sponsor
Kerman University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
2
Inclusion Criteria

Rural cutaneous leishmaniasis patient
Cutaneous leishmaniasis patients who have failed standard Glucantim treatment are included in the study

Exclusion Criteria

Acute infections
severe anemia
allergy
hemophilia
Immune system suppression
Skin malignancy
Low blood pressure
pregnancy
Anemia
Diabetes Type 1
Allergy to insect bites

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Wound healing time. Timepoint: Week. Method of measurement: Week.;Duration of infection. Timepoint: Week. Method of measurement: Week.;Complete healing of the wound. Timepoint: Week. Method of measurement: Week.
Secondary Outcome Measures
NameTimeMethod
Wound recurrence. Timepoint: Week. Method of measurement: Week.
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