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
| Type | Name | Description |
|---|---|---|
| DRUG | Pentoxifylline | Patients 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. |
| DRUG | Placebo | Patients 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.