Study of the Efficacy of Daylight Activated Photodynamic Therapy in the Treatment of Cutaneous Leishmaniasis
Primary Purpose
Cutaneous Leishmaniasis
Status
Unknown status
Phase
Phase 2
Locations
Israel
Study Type
Interventional
Intervention
Photodynamic therapy
Cryotherapy
Sponsored by
About this trial
This is an interventional treatment trial for Cutaneous Leishmaniasis focused on measuring Cutaneous leishmaniasis, Photodynamic therapy
Eligibility Criteria
Inclusion Criteria:
- At least 2 skin lesions with leishmania caused by L. major or L. tropica
Exclusion Criteria:
- Pregnant or lactating women
Sites / Locations
- Hadassah Medical Organization
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
1 PDT
Cryo
Arm Description
Leishmania lesion
Leishmania lesion
Outcomes
Primary Outcome Measures
Eradiation of amastigotes
Secondary Outcome Measures
Clinical healing
Full Information
NCT ID
NCT00840359
First Posted
February 8, 2009
Last Updated
August 15, 2011
Sponsor
Hadassah Medical Organization
1. Study Identification
Unique Protocol Identification Number
NCT00840359
Brief Title
Study of the Efficacy of Daylight Activated Photodynamic Therapy in the Treatment of Cutaneous Leishmaniasis
Official Title
Phase 2 Study of the Efficacy of Daylight Activated Photodynamic Therapy in the Treatment of Cutaneous Leishmaniasis
Study Type
Interventional
2. Study Status
Record Verification Date
August 2011
Overall Recruitment Status
Unknown status
Study Start Date
September 2009 (undefined)
Primary Completion Date
October 2012 (Anticipated)
Study Completion Date
December 2012 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
Hadassah Medical Organization
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The aim of the project is to determine whether daylight activated photodynamic therapy is effective in treating cutaneous leishmaniasis caused by L. major and L. tropical.
PDT is classically performed as a two-step procedure in which MAL application to the lesion constitutes the first step, and PpIX activation by light of appropriate wavelength from an artificial light source constitutes the second step. Based on the knowledge that red and blue light required to activate PpIX are part of the daylight spectrum, the investigators postulated that effective PpIX activation can be obtained by exposure of the MAL treated lesions to daylight thus substantially simplifying the PDT procedure by omitting the 3 hour incubation period and the subsequent exposure to artificial light. In accord, in a recent study the investigators showed that daylight-activated PDT (DA-PDT) was as effective as conventional MAL-PDT in treating precancerous actinic keratoses lesion. Furthermore the investigators found that DA-PDT is significantly less painful than conventional MAL-PDT.
The investigators now propose to study the efficacy of DA-PDT in the treatment of cutaneous leishmaniasis. DA-PDT has obvious advantages to conventional leishmania treatment forms:
As opposed to most of the available treatment options, DA-PDT is a self-administered procedure that does not require the assistance of medical personnel. Secondly, judged by our experience with MAL-PDT, only few treatment sessions are required for effective parasite killing as opposed to the prolonged procedures usually required for treatment of leishmaniasis. Third, PDT has the far the best safety profile of all available treatment options.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cutaneous Leishmaniasis
Keywords
Cutaneous leishmaniasis, Photodynamic therapy
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
44 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
1 PDT
Arm Type
Experimental
Arm Description
Leishmania lesion
Arm Title
Cryo
Arm Type
Active Comparator
Arm Description
Leishmania lesion
Intervention Type
Procedure
Intervention Name(s)
Photodynamic therapy
Intervention Description
Application of Metvix 16% cream followed by exposure to daylight for 2.5 hours
Intervention Type
Procedure
Intervention Name(s)
Cryotherapy
Intervention Description
Cryotherapy for 2 times 20 sec
Primary Outcome Measure Information:
Title
Eradiation of amastigotes
Time Frame
3 months following last treatment session
Secondary Outcome Measure Information:
Title
Clinical healing
Time Frame
3 months following last treatment session
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
At least 2 skin lesions with leishmania caused by L. major or L. tropica
Exclusion Criteria:
Pregnant or lactating women
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Claes D Enk, MD, PhD
Organizational Affiliation
Hadassah Medical Organization
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hadassah Medical Organization
City
Jerusalem
ZIP/Postal Code
IL-91010
Country
Israel
12. IPD Sharing Statement
Learn more about this trial
Study of the Efficacy of Daylight Activated Photodynamic Therapy in the Treatment of Cutaneous Leishmaniasis
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