Tracking Information

First Submitted Date ^ICMJE

July 1, 2019

First Posted Date ^ICMJE

July 5, 2019

Last Update Posted Date

May 27, 2021

Actual Study Start Date ^ICMJE

February 15, 2019

Estimated Primary Completion Date

September 1, 2021 (Final data collection date for primary outcome measure)

Current Primary Outcome Measures ^ICMJE

Percent Change in Pain Rating on the Visual Analog Scale (VAS) [ Time Frame: Baseline and 6 weeks ]

The Visual Analog Scale (VAS) assesses level or degree of pain. It is a horizontal line anchored on the left by the label '0: no pain at all' and on the right by the label '100: worst pain imaginable'. The subject marks a location on the 0-100 line that appears to represent any level of pain he or she is experiencing at that time. This marking is measured with a 0 to 100 mm ruler and the number recorded. For the primary study outcome, the percent change in the VAS pain score recorded at baseline and endpoint is calculated for each subject. Individual subject success is a 30% or greater change in VAS pain scores. A negative (-) percent change indicates a decrease in pain level and is positive for individual subject success. A positive (+) percent change indicates an increase in pain level and is negative for individual subject success. Overall study success is defined as a 35% or greater difference between the proportion of individual successes in each treatment group.

Original Primary Outcome Measures ^ICMJE

Percent Change in Pain Rating on the Visual Analog Scale (VAS) [ Time Frame: Baseline and 6 weeks ]

Percent change in pain score on the Visual Analog Scale (VAS) from baseline to endpoint measurement is calculated for each subject. Individual subject success is defined as a 30% or greater change in VAS pain scores across the evaluation period. A negative (-) percent change indicates a decrease in pain level and is positive for individual subject success. A positive (+) percent change indicates an increase in pain level and is negative for individual subject success. Overall study success is defined as a 35% or greater difference between the proportion of individual successes in each treatment group.

Change History

Current Secondary Outcome Measures ^ICMJE

Difference in Rescue Pain Medication Use [ Time Frame: Baseline and 6 weeks ]
Evaluation of the differences in the frequency of use of standardized study pain relief medication for foot pain during the study duration, measured as the total number of doses of rescue pain medication taken across the 6-week evaluation period.
Change in Total Score on the Neuropathic Pain Symptom Inventory (NPSI) [ Time Frame: Baseline and 6 weeks ]
The Neuropathic Pain Symptom Inventory (NPSI) is a 12-item self-administered patient-reported outcome (PRO) assessment tool to evaluate symptoms of neuropathic pain in adults over the past 24 hours. There are 10 descriptors representing 5 dimensions: burning pain, deep pain, paroxysmal pain, evoked pain, paresthesia/dysesthesia, and 2 temporal items. Each item is rated on a 0 to 10 scale where '0' means the item is not present at all and '10' means it is the worst possible presentation of the item. Responses to the individual items are added to get a total score. The higher the total score, the worst the subject's symptoms of neuropathic pain. The lower the total score, the lesser the symptoms. Therefore, an increase in the total score indicates a worsening of symptoms and a decrease in the total score indicates an improvement in symptoms.

Original Secondary Outcome Measures ^ICMJE

Difference in Rescue Pain Medication Use [ Time Frame: Baseline and 6 weeks ]
Evaluation of the differences in the frequency of use of standardized study pain relief medication for foot pain during the study duration, measured as the total number of doses of rescue pain medication taken across the 6-week evaluation period.
Change in Total Score on the Neuropathic Pain Symptom Inventory (NPSI) [ Time Frame: Baseline and 6 weeks ]
The Neuropathic Pain Symptom Inventory (NPSI) evaluates the different symptoms of neuropathic pain in adults. It is a 12-item self-administered patient-reported outcome (PRO) assessment tool with a recall/observation period of over the past 24 hours. It contains 10 descriptors representing 5 distinct dimensions on the basis of factor analysis: burning pain, deep pain, paroxysmal pain, evoked pain, paresthesia/dysesthesia, and 2 temporal items designed to assess pain duration and the number of pain paroxysms. Responses to each of the items are added to get a total score.

Current Other Pre-specified Outcome Measures

Not Provided

Original Other Pre-specified Outcome Measures

Not Provided

Descriptive Information

Brief Title ^ICMJE

An Evaluation of the Effect of Low Level Laser Therapy on Diabetic Peripheral Neuropathy Pain

Official Title ^ICMJE

A Double-blind, Placebo-controlled Randomized Evaluation of the Effect of the Erchonia® FX-635™ on Diabetic Peripheral Neuropathy Pain

Brief Summary

The purpose of this study is to determine whether low level laser therapy is effective in the reduction of foot pain associated with diabetic peripheral neuropathy.

Detailed Description

Peripheral neuropathy is one of the most common chronic diseases and a leading cause of adult disability in the U.S. Diabetic neuropathy represents over a third of all neuropathies, making diabetes the leading cause of peripheral neuropathy, affecting about 15-18 million Americans.

Living with neuropathy can cause tremendous frustration and social isolation. The daily chronic pain impacts day-to-day functionality resulting in physical and psychological problems including impaired concentration, anxiety, depression, a decline in cognitive abilities, and sleep difficulties which in turn can lead to irritability and increased pain sensitivity. Additionally, the economic burden from medical costs and workplace productivity losses are high and on the rise as the incidence of peripheral neuropathy increases.

Peripheral neuropathy describes damage to the peripheral nervous system that interferes with vital nerve connections, distorting and sometimes interrupting messages between the brain and the rest of the body. Diabetic peripheral neuropathy is a chronic acquired form of nerve damage that can occur in individuals with diabetes wherein the primary cause is damage to nerve fibers and blood vessels from prolonged exposure to high blood sugar (glucose). While the precise mechanism for this damage remains unclear, a combination of factors likely plays a role, including the complex interaction between nerves and blood vessels. High blood glucose interferes with the ability of the nerves to transmit signals and weakens the walls of the small blood vessels (capillaries) that supply the nerves with oxygen and nutrients.

The primary and most debilitating symptom of diabetic peripheral neuropathy is a sensation of tingling, prickling, buzzing, pinching, burning, and/or sharp jabbing stabbing pain in the feet. Nerve pain from diabetic peripheral neuropathy can be severe, constant, and difficult to treat. Current therapies include an array of over-the-counter and prescription medications or alternative treatment options such as injections or patches of local anesthetics; surgical destruction of nerves; implantation of a device to relieve pain; transcutaneous electrotherapy (TENS); hand or foot braces and orthopedic shoes.

Low Level Laser Therapy (LLLT) communicates information to the receptors on the membrane of the cell and mitochondrion (the enzymatic engine of the cell). This energetic information reaches the cell's DNA, which directly controls cell function. When the cells receive better information, they work better, as do the tissues they comprise, like bones, cartilage, tendons, ligaments, etc. In this way, LLLT promotes the healing and regeneration of damaged tissues, having both local effects on tissue function and also systemic effects carried throughout the body by the blood and acupuncture meridians.

The key basic physiological effects of low level laser light include increased cell membrane polarization and permeability; Adenosine-5-triphosphate (ATP) production and respiratory chain activity; enzyme activity; collagen and epithelial production; capillary formation; macrophage (immune) activity; analgesic effects due to elevated endorphin production, electrolytic nerve blockage, and improved blood and lymph flow; anti-inflammatory effect due to improved circulation and accelerated tissue regeneration; and increased production of antioxidants. Of additional benefit is that light energy from low level lasers will only be absorbed by cells and tissues that are not functioning normally and has no effect on healthy cells.

Therefore, low level laser therapy has the potential benefit of providing an effective means of reducing low back pain that is simple, quick, non-invasive and side-effect free.

Study Type ^ICMJE

Interventional

Study Phase ^ICMJE

Not Applicable

Study Design ^ICMJE

Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose: Treatment

Condition ^ICMJE

Diabetic Peripheral Neuropathy

Intervention ^ICMJE

Device: Erchonia FX-635
The Erchonia FX-635 has three independent 17 milliWatts (mW) 635 nanometer (nm) red laser diodes mounted in scanner devices.
Device: Placebo Laser
Non-therapeutic output.

Study Arms ^ICMJE

Experimental: Erchonia FX-635
The Erchonia FX-635 is administered to the foot 12 times over 6 weeks (2 times each week) for 15 minutes per foot.

Intervention: Device: Erchonia FX-635
Sham Comparator: Placebo Laser
Noise and appearance of output is the same but no active therapy applied. Treatment administration procedure is the same as with the experimental arm.

Intervention: Device: Placebo Laser

Publications *

Not Provided

* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.

Recruitment Information

Recruitment Status ^ICMJE

Active, not recruiting

Actual Enrollment ^ICMJE

14

Original Estimated Enrollment ^ICMJE

64

Estimated Study Completion Date ^ICMJE

October 1, 2021

Estimated Primary Completion Date

September 1, 2021 (Final data collection date for primary outcome measure)

Eligibility Criteria ^ICMJE

Inclusion Criteria:

18 years of age or older. Significant spontaneous pain of 50 or greater on the 0-100 VAS for the feet overall.
Existing clinical diagnosis of diabetes induced Peripheral Neuropathy.
Significant spontaneous foot pain that occurs comparably bilaterally.
Foot pain is chronic, ongoing for at least 3 months, bilaterally.
Subject has been on a stable anti-diabetic medication regimen or on no anti-diabetic medication regimen for the prior 30 days.
Subject has not used or is willing to abstain from using analgesics within 7 days prior to study start.
Subject has been on a stable dosage of antidepressants for at least 90 days prior to study start and is willing and able to maintain that stable dosage throughout study participation OR subject has not used or is willing to abstain from using antidepressants for 30 days prior to study start.
Subject has been on a stable dosage of any of Neurontin, Lyrica, Tramadol and Opioid medicines such as Ultram and Ultracet for at least 90 days prior to study start and is willing and able to maintain that stable dosage throughout study participation OR subject has not used or is willing to abstain from using any of the these medications for 30 days prior to study start.
Subject has not received or is willing to abstain from receiving any injections of local anesthetics such as lidocaine within 30 days prior to study start.
Subject is able and willing to take over-the-counter Regular Strength Tylenol tablets to manage pain, as needed, throughout the study.
Subject is willing and able to refrain from consuming any over-the-counter and/or prescription medications including muscle relaxants and/or herbal supplements and/or recreational and medical drugs including cannabis intended for the relief of pain and/or inflammation throughout study participation, except for the study-specific pain relief medication of over-the-counter Tylenol.
Subject is willing and able to refrain from engaging in any non-study procedure therapies for the management of foot pain throughout the study, including conventional therapies such as physical therapy, occupational therapy and hot or cold packs, as well as alternative therapies such as chiropractic care and acupuncture.
Can communicate fluently in English and can read and write English sufficiently to comply with the study procedures and complete the information in the Subject Diary.

Exclusion Criteria:

Subject's foot pain is undiagnosed, or has been diagnosed as being other than, or in addition to, diabetes induced Peripheral Neuropathy.
Subject's foot pain is unilateral or notably different between the two feet.
Serious organ disease or other serious primary disease merger.
Diabetes ketosis, ketoacidosis or severe infection within the past two weeks.
Current, active chronic pain disease: chronic fatigue syndrome, fibromyalgia, endometriosis, inflammatory bowel disease, interstitial cystitis, peripheral vascular disease.
Cancer or treatment for cancer in the past 6 months.
Surgical intervention to treat diabetic peripheral neuropathy foot pain, including implantation of a pain relief device.
Active infection, wound, or other external trauma to the areas to be treated with the laser.
Medical, physical, or other contraindications for, or sensitivity to, light therapy.
Pregnant, breast feeding, or planning pregnancy prior to the end of study participation.
Serious mental health illness such as dementia or schizophrenia; psychiatric hospitalization in past two years.
Developmental disability or cognitive impairment that in the opinion of the investigator would preclude adequate comprehension of the informed consent form and/or ability to record the necessary study measurements.
Any condition or other variable that in the opinion of the investigator may confound or interfere with the evaluation of the effectiveness of the investigational treatment or otherwise render the subject unable to comply with the requirements of the study protocol.
Involvement in litigation and/or receiving disability benefits related in any way to the parameters of the study.
Participation in a clinical study or other type of research in the past 30 days.

Sex/Gender ^ICMJE

Sexes Eligible for Study:

All

Ages ^ICMJE

18 Years and older (Adult, Older Adult)

Accepts Healthy Volunteers ^ICMJE

No

Contacts ^ICMJE

Contact information is only displayed when the study is recruiting subjects

Listed Location Countries ^ICMJE

United States

Removed Location Countries

Administrative Information

NCT Number ^ICMJE

NCT04006392

Other Study ID Numbers ^ICMJE

EC_DPN2

Has Data Monitoring Committee

No

U.S. FDA-regulated Product

Studies a U.S. FDA-regulated Drug Product:	No
Studies a U.S. FDA-regulated Device Product:	Yes
Product Manufactured in and Exported from the U.S.:	No

IPD Sharing Statement ^ICMJE

Not Provided

Responsible Party

Erchonia Corporation

Study Sponsor ^ICMJE

Erchonia Corporation

Collaborators ^ICMJE

Not Provided

Investigators ^ICMJE

Principal Investigator:

Sandra L Franco, DPM

PRS Account

Erchonia Corporation

Verification Date

May 2021

^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP

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An Evaluation of the Effect of Low Level Laser Therapy on Diabetic Peripheral Neuropathy Pain

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