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Clinical Trial Summary

The purpose of this protocol is to conduct a randomized comparison of the efficacy and tolerance of miltefosine, LAMB, and pentavalent antimony for the treatment of mucosal leishmaniasis. With such controlled pharmacodynamic data, and additional considerations of administrative convenience (oral >>IV) and cost, we hope that it will be possible for policy makers, treatment professionals, and patients to choose the most appropriate therapy for ML.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04799236
Study type Interventional
Source Fundacion Nacional de Dermatologia
Contact jaime soto, MD
Phone +59175648894
Email jasm.dlb@gmail.com
Status Recruiting
Phase Phase 3
Start date April 1, 2021
Completion date November 30, 2024

See also
  Status Clinical Trial Phase
Recruiting NCT01301937 - Low Antimonial Dosage in American Mucosal Leishmaniasis Phase 2/Phase 3
Completed NCT01050907 - Miltefosine to Treat Mucocutaneous Leishmaniasis Phase 2