Comparison of two regimens of fluconazol in treatment of cutaneous lieshmaniasis

Phase 2

• Conditions: Cutaneous leishmaniasis; Cutaneous leishmaniasis.

• Registration Number: IRCT138710221542N1
• Lead Sponsor: Shiraz University of Medical Scienses

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: 94

Inclusion Criteria

age over 12 years, positive PCR for leishmanisis and no treatment in two months ago, duration of disease is lower than 4 months.
Exclusion criteria: pregnancy, breast feeding, possibility of pregnancy in future, number of lesion over ten, history of liver disease and high BUN or Cr.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Reepithelialization. Timepoint: every two week. Method of measurement: observation.;Size of lesion. Timepoint: every two week. Method of measurement: with ruler.;Induration of lesion. Timepoint: every two week. Method of measurement: physical examination.

Secondary Outcome Measures

Name	Time	Method
Rising of liver enzyme, BUN and Cr. Timepoint: every two week. Method of measurement: Blood sample and laboratory measurment.;Nausea and vomitting. Timepoint: every two week. Method of measurement: History.