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CompletedNCT02588599Updated Sep 28, 2016Results posted

A Retrospective Analysis of the Effects of Low Level Laser Therapy on Toenail Onychomycosis

An interventional study of Erchonia LUNULA in Onychomycosis, sponsored by Erchonia Corporation. Completed. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2016-09-28.

Sponsored by Erchonia Corporation · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
54
Allocation
Not applicable
Ages
18 Years and older
Sex
All
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Study summary

The purpose of this study is to determine whether low level laser therapy (LLLT) using the Erchonia LUNULA device is effective in increasing clear nail in toenails with onychomycosis.

Read the detailed description

Nail onychomycosis, or fungus infection, is typically caused by a fungus called dermatophytes, but may also be caused by yeasts and molds. These microscopic organisms invade the skin through tiny invisible cuts or through a small separation between the nail and the nail bed. Under conditions of warmth and moisture, the fungi grow and spread. The infection begins as a white or yellow spot under the tip of the nail, and as it spreads deeper into the nail, causes unsightly and potentially painful nail discoloration, thickening and the development of crumbling edges. Onychomycosis occurs more commonly in toenails than in fingernails because toenails are often confined in a dark, warm, moist environment inside shoes where fungi can thrive. Toenail fungus affects approximately 23 million people in the US - about 10% of all adults.

Potential complications of onychomycosis include pain in the nails, permanent damage to the nails, development of other serious infections that can spread beyond the feet for individuals with a suppressed immune system due to medication, diabetes or other conditions, such as leukemia and AIDS.

Nail fungus can be difficult to treat, and repeated infections are common. Currently available treatments for onychomycosis include oral antifungal medications, antifungal lacquer, and topical medications, surgical nail removal and photodynamic therapy.

There is no perfect cure for toenail fungus. Even the most effective oral medications are successful only about half of the time, and topical medications are successful less than 10% of the time. Recently, research has found laser therapy to show promise as a novel alternative treatment for toenail onychomycosis. Unlike medication-driven treatments for toenail fungus which can have many side effects including serious ones such as liver toxicity, laser therapy presents minimal to no risk of side effects. Laser therapy is applied to toenail onychomycosis by shining a laser light through the toenail into the tissue below. The laser light vaporizes the fungus while leaving the skin and surrounding healthy tissue unharmed.

Low level laser therapy operates under the principle of photochemistry with a photoacceptor molecule absorbing the emitted photons and inducing a biological cascade. Like our eukaryotic cell, fungi contain the highly complex organelle the mitochondria, which is responsible for the manufacturing of the energy molecule adenosine triphosphate (ATP). Within the inner mitochondrial membrane is cytochrome c oxidase, an identified photoacceptor molecule. It is believed that laser therapy could perhaps provide a means to photo-destroy the fungi responsible for onychomycosis (OM) by inducing the release of highly reactive superoxides. Moreover, laser therapy has been shown to promote superoxide dismutase (SOD), a process responsible for the destruction of foreign invaders. Extracellular release of low levels of mediators associated with SOD can increase the expression of chemokines, cytokines, and endothelial leukocyte adhesion molecules, amplifying the cascade that elicits the inflammatory response. The physiologic function of hydrogen peroxide, superoxide anion, and hydroxyl free radical is to destroy phagocytosed microbes. By enhancing the natural processes of the immune system and impacting the structural integrity of the fungi strain, it is believed that laser therapy may provide a means for clinicians to effectively treat OM without the onset of any adverse events.

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Conditions studied

  • Onychomycosis

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03

In context

Onychomycosis

147 studies on the registry are indexed under Onychomycosis; 13 are open to participants now.

This study's enrollment of 54 is close to the median of 56 across 134 interventional studies indexed under Onychomycosis.

Browse Onychomycosis studies →

Lead sponsor

Erchonia Corporation is the lead sponsor of 48 studies on the registry; 2 are open to participants now.

Of its 14 completed or terminated interventional studies of FDA-regulated products, 14 (100%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Great toenail presents with clearly visually identifiable and photographically documentable onychomycosis of the great toenail, or no visible onychomycosis (1 great toenail)
  • Onychomycosis has been identified as due to bacterial/fungal infection classified by the investigator as onychomycosis, with the nail presenting positive on visual inspection for somewhat thickened nail plate with a cloudy appearance and some discoloration (white to yellow to brown)
  • Onychomycosis etiology has been confirmed through positive fungal potassium hydroxide preparation (KOH) testing results

Exclusion criteria

Exclusion Criteria:

  • Spikes of disease extending to nail matrix in the great toenail
  • Infection involving lunula of the great toenail, e.g. genetic nail disorders, primentary disorders
  • Great toenail has less than 2mm clear (unaffected) nail plate length beyond the proximal fold
  • Dermatophytoma or "yellow spike/streak" (defined as thick masses of fungal hyphae and necrotic keratin between the nail plate and nail bed) on the great toenail
  • Onychogryphosis
  • Proximal subungual onychomycosis
  • White superficial onychomycosis
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
54 participants (actual)

Study arms

  • Experimental
    Erchonia LUNULA

    The Erchonia LUNULA emits both red light (635 nm) and blue light (405 nm) to the affected toenail for 12 minutes per treatment for 4 treatments, each treatment one week apart.

    Device: Erchonia LUNULA

Interventions

  • DeviceErchonia LUNULA

    Active low level laser light therapy

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What researchers measure

Primary outcomes

  1. Percent (%) of Toenails Attaining 3 Millimeters (mm) or More of Clear Nail Growth

    Individual toenail success criteria was defined as 3 millimeter (mm) or more of clear nail growth at 6 months post-procedure administration as evaluated relative to baseline. Overall study success criteria was defined as an 60% or more of treated toenails meeting the individual success criteria.

    Time frame: 6 Months

Secondary outcomes

  1. Change in Millimeters (mm) of Clear Nail Bed

    Millimeter (mm) of clear nail from the base of the toenail was determined from digital photographs of the toenail using a computer program. Change in mm of clear nail bed was calculated as the difference in mm of clear nail bed from baseline measurement to the measurement at 6 months after the end of the procedure administration phase. An increase in mm of clear nail between the two measurement points indicates that the toenail has improved and is positive for study success. A decrease in mm of clear nail between the two measurement points indicates that the toenail has worsened and is negative for study success.

    Time frame: Baseline and 6 Months

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Results

Posted Jul 21, 2016

Participant flow

Participant flow — Overall Study
MilestoneErchonia LUNULA
Started54
Completed54
Not completed0

Outcome measures

PrimaryPercent (%) of Toenails Attaining 3 Millimeters (mm) or More of Clear Nail Growth

Individual toenail success criteria was defined as 3 millimeter (mm) or more of clear nail growth at 6 months post-procedure administration as evaluated relative to baseline. Overall study success criteria was defined as an 60% or more of treated toenails meeting the individual success criteria.

Time frame:
6 Months
Reported as:
Number · Percent of Toenails
Percent (%) of Toenails Attaining 3 Millimeters (mm) or More of Clear Nail Growth
Percent of ToenailsErchonia LUNULA
Percent (%) of Toenails Attaining 3 Millimeters (mm) or More of Clear Nail Growth67
SecondaryChange in Millimeters (mm) of Clear Nail Bed

Millimeter (mm) of clear nail from the base of the toenail was determined from digital photographs of the toenail using a computer program. Change in mm of clear nail bed was calculated as the difference in mm of clear nail bed from baseline measurement to the measurement at 6 months after the end of the procedure administration phase. An increase in mm of clear nail between the two measurement points indicates that the toenail has improved and is positive for study success. A decrease in mm of clear nail between the two measurement points indicates that the toenail has worsened and is negative for study success.

Time frame:
Baseline and 6 Months
Reported as:
Mean · millimeters
Change in Millimeters (mm) of Clear Nail Bed
millimetersErchonia LUNULA
Change in Millimeters (mm) of Clear Nail Bed5.18 ± 4.76
Statistical analysis
  • Erchonia LUNULA · t-test, 2 sided · p = <0.0001t=8.0; df=53

Adverse events

Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Erchonia LUNULA—0/54 (0%)0/54 (0%)

Baseline characteristics

Age, Categorical
Age, Categorical(Participants)Erchonia LUNULA
<=18 years0
Between 18 and 65 years54
>=65 years0
Sex: Female, Male
Sex: Female, Male(Participants)Erchonia LUNULA
Female30
Male24
08

Study locations

No study locations are listed for this record.

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References and documents

Publications

  • Zang K, Sullivan R, Shanks S. A Retrospective Study of Non-thermal Laser Therapy for the Treatment of Toenail Onychomycosis. J Clin Aesthet Dermatol. 2017 May;10(5):24-30. Epub 2017 May 1. PubMed 28670355 ↗

Individual participant data

Plan to share: No

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 28, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02588599
Lead sponsor
Erchonia Corporation
Responsible party
Sponsor
First posted
Oct 28, 2015
Start date
Oct 2015
Primary completion
Oct 2015
Completion
Oct 2015
Results posted
Jul 21, 2016
Last update
Sep 28, 2016

Study contacts

Kerry Zang, DPM
principal investigator

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2016. You cannot join it, but the record below documents what was studied.

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