High Intensity LED Photobiomodulation Therapy for Chronic Leg and Foot Ulcers
NCT ID: NCT04300205
Last Updated: 2023-09-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
33 participants
INTERVENTIONAL
2020-02-25
2022-06-25
Brief Summary
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Detailed Description
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Hypothesis: Patients with chronic diabetic or venous foot/leg ulcers treated with standard care plus 10 minutes of high intensity LED light therapy will experience less overall pain associated with their ulcer and the ulcer will heal faster than standard care alone.
Justification: Diabetic and venous foot ulcers are debilitating, costly, extremely painful and interfere significantly with quality of life. Standard care for chronic wounds has improved but there is great need of new treatments to complement wound care, reduce pain, and accelerate wound healing. High intensity LED light therapy is a re-emerging treatment option that is known to decrease inflammation, decrease pain, and increase tissue regeneration.
Objectives: The primary objective is to assess the safety of a high intensity LED light device (KPTL-10) in the treatment of chronic foot and leg ulcers. The secondary objectives are to assess the ability of the KPTL-10 device to reduce pain and accelerate wound healing.
Research Method/Procedures: Participants with chronic foot and leg ulcers less than 8 cm in diameter (longest direction) will randomized into one of 2 groups for this study: 1) to receive a free 10 minute light treatment with the KPTL10 device in addition to standard care, or 2) strictly be a part of the standard care control group (no light treatment). For treatment, the light device is placed at a fixed distance (1 cm) above the wound. All participants will have wound measurements taken with digital software throughout the course of the study to track wound healing. Patients will also record their pain levels by filling out a VAS pain scale throughout the study.
Plan for Data Analysis: For each study participant, detailed Case Report Forms will be completed by study researchers and the principal investigator Dr. Eric Bly at every study appointment. The target numbers for this study data set are 40 treated participants, and 20 control (untreated) participants. These case report forms contain data sections to capture wound sizes, patient experiences post treatment, and pain scores (VAS scale). All data will be stored digitally on a single study computer and manually as printed hardcopies for study records and complete data analysis by Dr. Eric Bly and Illumacell's clinical team.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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High intensity LED light treatment
Participants treated with high intensity LED phototherapy
High intensity LED light device
Participant wounds are treated with LED light device for 10 minutes, 4 times over the course of 2 months
Sham high intensity LED light treatment
Participants set up to be treated with light device but after being masked, the device is moved off the wound
Sham LED light device
Participants have the light treatment moved off their wound after masking
Interventions
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High intensity LED light device
Participant wounds are treated with LED light device for 10 minutes, 4 times over the course of 2 months
Sham LED light device
Participants have the light treatment moved off their wound after masking
Eligibility Criteria
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Inclusion Criteria
* healable wounds
* non-cancerous wounds
Exclusion Criteria
* participants taking photosensitive drugs for concomitant disease
18 Years
ALL
No
Sponsors
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Kerber Applied Research
UNKNOWN
Alberta Health Services - Lower Limb Wound Clinic
UNKNOWN
Illumacell Inc.
INDUSTRY
Responsible Party
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Principal Investigators
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Jeff Hummel, PhD
Role: STUDY_DIRECTOR
Illumacell Inc.
Locations
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Alberta Health Services - Lower Limb Wound Care
Lethbridge, Alberta, Canada
Countries
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Related Links
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Website contains Abstract and Data Summary for "ILLUMACELL AND AHS PROFESSIONAL SUMMARY OF WOUND CARE ALBERTA (WCAB) STUDY"
Other Identifiers
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WCAB-89340
Identifier Type: -
Identifier Source: org_study_id
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