Evaluation of PDL laser for the treatment of cutaneous leishmaniasis

Phase 2

• Conditions: Cutaneous leishmaniasis.; Cutaneous leishmaniasis

• Registration Number: IRCT2014072018536N1
• Lead Sponsor: Dr Radmanesh clinic

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 38

Inclusion Criteria

Age between 5-55 years; having at least 2 leishmania lesion on the everywhere of body skin with positive direct smear for leishman body.
Exclusion criteria: Pregnancy; lactation; using any other treatments before the beginning of the study.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Induration index. Timepoint: Before the begionning of the study, Every 2 weeks for 10 weeks. Method of measurement: Physical examination by dermatologist.

Secondary Outcome Measures

Name	Time	Method
Post inflammatory hyperpigmantation. Timepoint: Every 2 weeks for 10 weeks. Method of measurement: Physical examination by dermatologist.