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Pilot Study Using a Heat Pack to Treat Cutaneous Leishmaniasis

Pilot Study of Thermotherapy Treatment for Cutaneous Leishmaniasis in Peru With the HECT-CL Device

Status
AVAILABLE
Phases
Unknown
Study type
Expanded Access
Source
ClinicalTrials.gov
Registry ID
NCT01277796
Acronym
HECT
Enrollment
Unknown
Registered
2011-01-17
Start date
Unknown
Completion date
Unknown
Last updated
2011-01-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cutaneous Leishmaniasis

Brief summary

Current standard therapies with chemotherapy (CT) for Cutaneous Leishmaniasis (CL) are expensive, toxic/allergenic, frequently ineffective, burdensome, and often unavailable. Thermotherapy is a clinically validated first line alternative for the treatment of Cutaneous Leishmaniasis in South America. However, current heat-delivery modalities are either too costly or lack governmental approval required to be made widely available to endemic areas. The investigators have adapted a reliable, safe, and low-cost heat pack for Cutaneous Leishmaniasis that the investigators have named the HECT-CL device. In this pilot study the investigators will enroll 25 patients who have either failed or are not candidates for pentivalent antimonies. The hypothesis states that the HECT-CL device demonstrates efficacy non-statistically inferior to estimates for current South American Pentavalent Antimonial cure rates (76%) while demonstrating basic safety and tolerability.

Interventions

DEVICEHeat pack conduction-heat therapy

Hand warmer heat pack with reliable (and monitored) temperature (50-52 degrees Celsius) will be applied to lesion borders for 3 minutes (fractionated to 90 second intervals or less) every day, for 7 consecutive days.

Sponsors

Tulane University School of Medicine
CollaboratorOTHER
Universidad Peruana Cayetano Heredia
Lead SponsorOTHER

Eligibility

Sex/Gender
ALL
Age
8 Years to 80 Years

Inclusion criteria

* with CL diagnosed by skin smear (WHO method), biopsy, culture, PCR * aged 8-80 years old * with no more than 3 lesions * ulcerative and non-ulcerative ulcers less than 4 cm diameter. * allergy, prohibitive side effects to standard chemotherapy, or other contraindication to antimonial treatment (e.g. cardiac arrhythmia) * capable of signing an informed consent or having capable guardians (in the case of minors). * Children ≥ 8 years of age must give written or verbal informed assent along with written consent of their guardians.

Exclusion criteria

* lesions less than 2cm from the nose, mouth, ears, or eyes. * clinically diagnosed with mucosal involvement. * evidence of lymph node involvement on exam. * unable or unwilling to commit to the treatment and follow-up plan. * prior CL treatment within last 1 month. * pregnant or lactating * uncontrolled severe systemic illness or immunocompromised state.

Contacts

Primary ContactAlejandro Llanos-Cuentas, MD, PhD
elmer.llanos@upch.pe51-1-482-7739

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026