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NCT07149753Possibly a fitNot yet recruiting

Miltefosine gel for skin sores from leishmaniasis

Cutaneous LeishmaniasisCutaneous Leishmaniasis, AmericanTopical Administration

Treatments studied

Part of Infections, Skin clinical trials.

This study tests a gel containing miltefosine (a medicine) applied directly to the skin sores caused by cutaneous leishmaniasis. The goal is to see if the gel is safe and works to clear the sores.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 1
Enrollment
15 people
Ages
18 years to 65 years
Study type
Interventional

Who can take part

  • You must be between 18 and 65 years old.
  • You must have a confirmed diagnosis of cutaneous leishmaniasis (a skin infection caused by a parasite).
  • You must have 1 to 4 skin sores, each about 1 to 4 cm in size, that have been present for more than a month, and they must NOT be on your face, ears, or joints.
  • You must not have the more serious forms of leishmaniasis (like mucosal or widespread disease).
  • You must not have had oral or injected anti-leishmaniasis treatment in the last 8 weeks, and you must not have failed earlier local treatments.
  • You cannot be pregnant or breastfeeding, and if you are of childbearing age, you must agree to use contraception during and for 45 days after treatment.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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