Onychomycosis Clinical Trial
Official title:
Pulsed Dye Laser Treatment of Onychomycosis
Verified date | August 2016 |
Source | Thomas Jefferson University |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
The purpose of this research is to investigate the use of the Candela V-beam Pulsed Dye
Laser for the treatment of onychomycosis, or nail fungus.
Hypothesis: Complete nail clearance will occur in approximately half of patients after 3
laser treatments.
Status | Completed |
Enrollment | 11 |
Est. completion date | July 2015 |
Est. primary completion date | December 2014 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Ages 18-65 years old - Diagnosis of onychomycosis based on positive fungal culture for dermatophyte and positive PAS from toenail clipping Exclusion Criteria: - HIV/immunosuppression - Candidal toenail infection - Prior PO antifungal therapy within last 6 months - Personal history of psoriasis, lichen planus, or significant photosensitivity disorder - Any serious generalized medical condition |
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | Jefferson Dermatology Associates | Philadelphia | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
Thomas Jefferson University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Total Nail Clearance | After 3 laser treatments, the subject should experience clinical clearance. | approximately 12 weeks | No |
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