Trials / Unknown
UnknownNCT02724384
Evaluating the Safety, Tolerability and Preliminary Efficacy of Plasma in Improving the Appearance of Onychomycosis
A Multi-Center Pilot Study to Evaluate the Safety, Tolerability and Preliminary Efficacy of the Plasma Treatment System in Improving the Appearance of Onychomycosis
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 75 (estimated)
- Sponsor
- Moe Medical Devices · Industry
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the safety and preliminary efficacy of using electrical plasma to treat toenail fungus.
Detailed description
75 patients will be recruited at several sites. Patients will be split into 3 groups that have different treatment doses. Patient participation in the study will last 12 months.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | MOE Plasma Delivery System A | Plasma treatment |
| DEVICE | MOE Plasma Delivery System B | Plasma treatment |
Timeline
- Start date
- 2016-03-01
- Primary completion
- 2018-12-01
- Completion
- 2019-02-01
- First posted
- 2016-03-31
- Last updated
- 2017-09-14
Locations
7 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT02724384. Inclusion in this directory is not an endorsement.