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LASER Pilot Project (LASER)

Primary Purpose

Acquired Absence of Lower Limb, Scar Condition and Fibrosis of the Skin

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Fractional CO2 Laser Ablative Resurfacing
Sponsored by
VA Office of Research and Development
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acquired Absence of Lower Limb focused on measuring Amputation, Scar, Fractional Ablative Laser Resurfacing

Eligibility Criteria

21 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Age 21-70 years. Lower extremity amputation at the transtibial or transfemoral levels. Lower extremity amputee who has regular and compliant use of a lower extremity prosthesis. Lower extremity prosthesis use is disrupted or complicated by scarring and other skin maladies treatable with fractional CO2 laser therapy. Cognitive ability to understand and willingness to provide informed consent and follow the study protocol. Willing and able to attend pre and post procedural assessment sessions. Willing and able to attend dermatologic and laser therapy sessions. Exclusion Criteria: Does not have lower extremity amputation. Lower extremity amputee who does not use a prosthesis. Lower extremity prosthetic use is not disrupted due to scarring or other skin maladies. Residual limb has an open wound or active infection. Has any of the following; open residual limb wound, cultured epithelial autographts, active infection, presence of unstable epithelium within the early weeks of injury Otherwise not a candidate for laser therapy.

Sites / Locations

  • Miami VA Healthcare System, Miami, FL
  • James A. Haley Veterans' Hospital, Tampa, FL

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Observational Single Arm

Arm Description

All subjects will have scars, quality of life, function assessed pre and post laser treatment

Outcomes

Primary Outcome Measures

Change in Prosthesis Evaluation Questionnaire
Patient Reported Outcome Measure with score from 0-100 with increased score demonstrated patient reported improvement
Change in 2 minute walk test
Functional performance with score from 0 - 999 feet with increased score demonstrating increased velocity in walking
Change in The Patient and Observer Scar Assessment Scale
Dermatologic Survey on a scale of 1-10 with increased number demonstrating worsening of scar appearance
Change in Optical Coherence Tomography
Observational Measure for documentation of scar characteristics
Change in Manchester Scar Scale
Dermatologic survey on a scale of 1-4 with higher numbers representing worsening of conditions of scar
Change in Dermatology Life Quality Index
Dermatologic survey using a scale from scar problems resulting in very much, a lot, a little or not at all impacts to quality of life
Change in Dermal Torque Meter
Observational Measure for documentation of scar characteristics
Change in Scar Photography
Observational Measure for documentation of scar characteristics
Change in Prosthesis Limb User Survey - Mobility
Patient reported outcome measure with scores from 20-80 with increase in score demonstrating increase in self reported functional mobility

Secondary Outcome Measures

Full Information

First Posted
July 18, 2023
Last Updated
September 6, 2023
Sponsor
VA Office of Research and Development
Collaborators
Miami Dermatology and Laser Institute, Bruce W. Carter VA Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT05966636
Brief Title
LASER Pilot Project
Acronym
LASER
Official Title
The LASER Pilot Project: Laser Therapy in Amputee Skin Care to Enhance Rehabilitation. A Preliminary InvestigationA
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 11, 2023 (Anticipated)
Primary Completion Date
August 31, 2025 (Anticipated)
Study Completion Date
August 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development
Collaborators
Miami Dermatology and Laser Institute, Bruce W. Carter VA Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Veterans who use prosthetic limbs commonly suffer from skin problems such as scars that create discomfort and pain to the point that wearing the prosthesis is no longer tolerable. The Veteran must then discontinue prosthetic use to allow healing prior to wearing the limb again. Current treatments for skin problems include manual scar mobilization and massage, stretching, desensitization techniques, pain medication, prosthetic adjustment, steroid injection, scar excision and others. Most of these have not proven to be a long-term solution. A dermatologic procedure common in non-amputees for scar and skin lesion management, fractionated laser therapy, may be a long-term solution minimizing discomfort, pain and time out of the prosthesis. This preliminary study seeks to determine if fractional laser therapy can improve prosthetic use, and quality of life of Veterans with amputation who use lower limb prostheses.
Detailed Description
Many Veterans with lower limb amputation who use prostheses suffer from skin related prosthetic fit issues such as scars. Problematic scars may be managed with surgical excision that can yield a larger, more sensitive scar. Massage and desensitization techniques are also options. These current interventions yield widely varied results based on many factors including clinician skill, which modality is selected, patient compliance and others. Prosthetic use, walking, training, scar steroid injection and other therapies are options for scar management today. Current scar management treatments are limited due to high variance in effectiveness. Fractionated CO2 laser treatment however is a proven intervention for scar treatment in non-amputee patients, such as those with limb salvage or burns. The overall goal of this preliminary study is to determine if fractionated CO2 laser therapy, may potentially improve outcomes in Veterans who use prostheses who have limitations due to problematic scars. In this preliminary investigation, the investigators will study the potential of fractionated CO2 laser therapy to decrease scar related discomfort, improve mobility and comfort otherwise restricted from problematic stump scarring and thus to improve quality of life. The investigators anticipate this will be a high-impact rapid translation intervention with the potential to restore functionality to individuals with lower limb amputation and transform the role of dermatologic care in lower limb prosthetics. The objective of this preliminary study is to explore the ability to recruit a sample of lower limb prosthesis users, coordinate laser therapy, collect outcomes and assure coordination and data fidelity between sites and facilitate determination of parameters for a future, more definitive clinical study of fractionated CO2 laser in the lower limb amputee population burdened with problematic scarring. The investigators' clinical hypothesis is fractionated CO2 laser treatment will provide considerable improvements in comfort, pain reduction, mobility and quality of life in lower limb prosthesis users. Further, it's hypothesize the investigators will be able to recruit a sample, assure data fidelity and be able to use the outcomes to estimate the power and sample to support a future clinical investigation and VA Merit application. Six to eight subjects will be recruited from the Tampa VA. They will receive a pre-procedural assessment including subjective and objective measures ultimately to measure functional mobility, socket comfort, prosthetic history, health related quality of life and residual limb measures (i.e. volumetrics, range of motion, muscle testing and others). Subjects will then be evaluated (including dermatologic outcome measures) by and receive laser therapy from a credentialed dermatologist and then return to the Tampa VA to repeat the aforementioned outcomes at 6 week, 3 months and 6 months follow ups. Following laser therapy, outcomes data will be analyzed to determine the treatment effect, power and ultimately, the necessary sample size for a future VA Merit proposal. Additionally, the study will provide preliminary evidence of efficacy of laser therapy in this population. It will also permit selection of the most ideal outcome measures and facilitate optimization of a protocol for the configuration of an optimized, more definitive study to determine efficacy of laser therapy in Veterans with lower limb amputation who use prostheses.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acquired Absence of Lower Limb, Scar Condition and Fibrosis of the Skin
Keywords
Amputation, Scar, Fractional Ablative Laser Resurfacing

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
The investigators will perform pre and post assessment of laser treatment techniques to improve scar mobility and skin health in a pilot sample of individuals with lower extremity limb loss who use artificial limbs for mobility.
Masking
None (Open Label)
Masking Description
Study statistician will be masked
Allocation
N/A
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Observational Single Arm
Arm Type
Other
Arm Description
All subjects will have scars, quality of life, function assessed pre and post laser treatment
Intervention Type
Procedure
Intervention Name(s)
Fractional CO2 Laser Ablative Resurfacing
Intervention Description
Fractional lasers stimulate scar improvement through production of microscopic patterns of dermal injury, vaporizing scar tissue and inducing neocollagenesis, subsequently improving scar tissue texture and range of motion, and decreasing symptoms such as pain and pruritis. Current clinical consensus is supportive that fractionated lasers are the most effective option for the treatment of scars. Other laser wavelengths and modalities used for vascular deformities and hair removal for instance, have an adjunctive role in improving scars and may be used in the same laser session. Case reports provide evidence of substantial improvement in sensory symptoms and physical mobility within days to weeks after each treatment.
Primary Outcome Measure Information:
Title
Change in Prosthesis Evaluation Questionnaire
Description
Patient Reported Outcome Measure with score from 0-100 with increased score demonstrated patient reported improvement
Time Frame
Baseline and post Treatment LASER Visit (week 6), and 3 and 6 month follow up visits
Title
Change in 2 minute walk test
Description
Functional performance with score from 0 - 999 feet with increased score demonstrating increased velocity in walking
Time Frame
Baseline and post Treatment LASER Visit (week 6), and 3 and 6 month follow up visits
Title
Change in The Patient and Observer Scar Assessment Scale
Description
Dermatologic Survey on a scale of 1-10 with increased number demonstrating worsening of scar appearance
Time Frame
Baseline and post Treatment LASER Visit (week 6), and 3 and 6 month follow up visits
Title
Change in Optical Coherence Tomography
Description
Observational Measure for documentation of scar characteristics
Time Frame
Baseline and post Treatment LASER Visit (week 6), and 3 and 6 month follow up visits
Title
Change in Manchester Scar Scale
Description
Dermatologic survey on a scale of 1-4 with higher numbers representing worsening of conditions of scar
Time Frame
Baseline and post Treatment LASER Visit (week 6), and 3 and 6 month follow up visits
Title
Change in Dermatology Life Quality Index
Description
Dermatologic survey using a scale from scar problems resulting in very much, a lot, a little or not at all impacts to quality of life
Time Frame
Baseline and post Treatment LASER Visit (week 6), and 3 and 6 month follow up visits
Title
Change in Dermal Torque Meter
Description
Observational Measure for documentation of scar characteristics
Time Frame
Baseline and post Treatment LASER Visit (week 6), and 3 and 6 month follow up visits
Title
Change in Scar Photography
Description
Observational Measure for documentation of scar characteristics
Time Frame
Baseline and post Treatment LASER Visit (week 6), and 3 and 6 month follow up visits
Title
Change in Prosthesis Limb User Survey - Mobility
Description
Patient reported outcome measure with scores from 20-80 with increase in score demonstrating increase in self reported functional mobility
Time Frame
Baseline and post Treatment LASER Visit (week 6), and 3 and 6 month follow up visits

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age 21-70 years. Lower extremity amputation at the transtibial or transfemoral levels. Lower extremity amputee who has regular and compliant use of a lower extremity prosthesis. Lower extremity prosthesis use is disrupted or complicated by scarring and other skin maladies treatable with fractional CO2 laser therapy. Cognitive ability to understand and willingness to provide informed consent and follow the study protocol. Willing and able to attend pre and post procedural assessment sessions. Willing and able to attend dermatologic and laser therapy sessions. Exclusion Criteria: Does not have lower extremity amputation. Lower extremity amputee who does not use a prosthesis. Lower extremity prosthetic use is not disrupted due to scarring or other skin maladies. Residual limb has an open wound or active infection. Has any of the following; open residual limb wound, cultured epithelial autographts, active infection, presence of unstable epithelium within the early weeks of injury Otherwise not a candidate for laser therapy.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Anita Ramrattan, DPT MS
Phone
(813) 558-3997
Email
anita.ramrattan@va.gov
First Name & Middle Initial & Last Name or Official Title & Degree
Jeffrey T Heckman, DO
Phone
(813) 972-2000
Ext
7506
Email
Jeffrey.T.Heckman@va.gov
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeffrey T Heckman, DO
Organizational Affiliation
James A. Haley Veterans' Hospital, Tampa, FL
Official's Role
Principal Investigator
Facility Information:
Facility Name
Miami VA Healthcare System, Miami, FL
City
Miami
State/Province
Florida
ZIP/Postal Code
33125
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ignacio Gaunaurd, PhD
Phone
305-206-2441
Email
ignacio.gaunaurd@va.gov
First Name & Middle Initial & Last Name & Degree
Luis Gonzalez, MBA
Phone
7867608959
Email
Luis.Gonzalez2@va.gov
Facility Name
James A. Haley Veterans' Hospital, Tampa, FL
City
Tampa
State/Province
Florida
ZIP/Postal Code
33612
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Briana N Chilton
Phone
813-558-7610
Email
Briana.Chilton@va.gov
First Name & Middle Initial & Last Name & Degree
Margaret R Covar
Phone
(813) 903-4407
Email
Margaret.Covar@va.gov
First Name & Middle Initial & Last Name & Degree
Jeffrey T Heckman, DO

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
There is no plan to share individual participant data beyond deidentified, group aggregated established scientific peer reviewed publication

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LASER Pilot Project

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