Diode Laser Treatment of Onychomycosis

This is an interventional device feasibility trial for Onychomycosis focused on measuring Onychomycosis, Toenail Fungus Read More

Inclusion Criteria:

• Confirmed subungual onychomycosis in a great toe that does not extend to the eponychium
• Fitzpatrick Skin Type I-IV
• Written and verbal informed consent
• Able to comply with study instructions and to return to the clinic for required visits
• Agrees to refrain from other active topical, laser or light-based treatment to the great toes
• Agrees to the use of Naftin Gel between the toes to prevent/control tinea pedis

Exclusion Criteria:

• Pregnancy, breastfeeding or planning to become pregnant
• History of cutaneous photosensitivity, porphyria and hypersensitivity to porphyrins or photodermatoses
• Any skin pathology or condition that could interfere with the evaluation or that requires the use of interfering topical or systemic therapy
• Coagulation disorder or current use of anti-coagulation medication (including aspirin use of greater than 81 mg per day)
• Any condition which, in the investigator's opinion, would make it unsafe for the subject to participate
• Enrolled in an investigational drug or device trial, or has been treated with an investigational device or received an investigational drug within 30 days
• Oral Lamisil within 1 year, Sporanox or over-the-counter topicals within 1 month, or other prescription anti-fungal medications or topicals within 6 months
• Evidence of diabetic neuropathy or peripheral vascular disease related to diabetes, or a loss of protective sensation in the affected foot
• Psoriasis, lichen planus, infection involving the lunula, prior surgical treatment of the affected great toe within 1 year, or a history of trauma to the affected great toe
• Immunocompromised status, or with existing (or history of) cancer/skin malignancy
• Distal nail thickness of greater than 2mm in the affected great toenail