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Pilot Study Using a Heat Pack to Treat Cutaneous Leishmaniasis (HECT)

Primary Purpose

Cutaneous Leishmaniasis

Status
Available
Phase
Locations
Study Type
Expanded Access
Intervention
Heat pack conduction-heat therapy
Sponsored by
Universidad Peruana Cayetano Heredia
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an expanded access trial for Cutaneous Leishmaniasis

Eligibility Criteria

8 Years - 80 Years (Child, Adult, Older Adult)All Sexes

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.

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Secondary Outcome Measures

    Full Information

    First Posted
    January 13, 2011
    Last Updated
    January 14, 2011
    Sponsor
    Universidad Peruana Cayetano Heredia
    Collaborators
    Tulane University School of Medicine
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    1. Study Identification

    Unique Protocol Identification Number
    NCT01277796
    Brief Title
    Pilot Study Using a Heat Pack to Treat Cutaneous Leishmaniasis
    Acronym
    HECT
    Official Title
    Pilot Study of Thermotherapy Treatment for Cutaneous Leishmaniasis in Peru With the HECT-CL Device
    Study Type
    Expanded Access

    2. Study Status

    Record Verification Date
    January 2011
    Overall Recruitment Status
    Available
    Study Start Date
    undefined (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    undefined (undefined)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Universidad Peruana Cayetano Heredia
    Collaborators
    Tulane University School of Medicine

    4. Oversight

    5. Study Description

    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.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Cutaneous Leishmaniasis

    7. Study Design

    8. Arms, Groups, and Interventions

    Intervention Type
    Device
    Intervention Name(s)
    Heat pack conduction-heat therapy
    Intervention Description
    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.

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    8 Years
    Maximum Age & Unit of Time
    80 Years
    Eligibility Criteria
    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.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Alejandro Llanos-Cuentas, MD, PhD
    Phone
    51-1-482-7739
    Email
    elmer.llanos@upch.pe
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Alejandro Llanos-Cuentas, MD, PhD
    Organizational Affiliation
    Universidad Peruana Cayetano Heredia
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Witzig Richard, MD, MPH
    Organizational Affiliation
    Tulane Medical School
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Pilot Study Using a Heat Pack to Treat Cutaneous Leishmaniasis

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