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
About this trial
This is an expanded access trial for Cutaneous Leishmaniasis
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.
Sites / Locations
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT01277796
First Posted
January 13, 2011
Last Updated
January 14, 2011
Sponsor
Universidad Peruana Cayetano Heredia
Collaborators
Tulane University School of Medicine
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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