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Trials / Completed

CompletedNCT01381055

Antimony Plus Pentoxifylline in Cutaneous Leishmaniasis

Double-blind Placebo Controlled Trial Using Pentoxifylline Associated With Pentavalent Antimony in Cutaneous Leishmaniasis

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
164 (actual)
Sponsor
Paulo Roberto Lima Machado · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether pentoxifylline associated to pentavalent antimony has a higher cure rate than pentavalent antimony alone in the treatment of cutaneous leishmaniasis.

Conditions

Interventions

TypeNameDescription
DRUGPentoxifyllinePatients with cutaneous leishmaniasis treated with pentavalent antimony/Meglumine antimoniate 20mg/kg/day during 20 days and pentoxifylline pills 400mg three times a day during 20 days.
DRUGPlaceboPatients with cutaneous leishmaniasis treated with pentavalent antimony/metilglucamine 20mg/kg/day during 20 days and placebo pills three times a day during 20 days.

Timeline

Start date
2012-03-01
Primary completion
2015-01-01
Completion
2015-10-01
First posted
2011-06-27
Last updated
2017-01-26

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT01381055. Inclusion in this directory is not an endorsement.

Antimony Plus Pentoxifylline in Cutaneous Leishmaniasis (NCT01381055) · Clinical Trials Directory