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Evaluating the Safety, Tolerability and Preliminary Efficacy of Plasma in Improving the Appearance of Onychomycosis

NCT02724384 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 75

Last updated 2017-09-14

No results posted yet for this study

Summary

The purpose of this study is to evaluate the safety and preliminary efficacy of using electrical plasma to treat toenail fungus.

Conditions

  • Onychomycosis

Interventions

DEVICE

MOE Plasma Delivery System A

Plasma treatment

DEVICE

MOE Plasma Delivery System B

Plasma treatment

Sponsors & Collaborators

  • Moe Medical Devices

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-03-31
Primary Completion
2018-12-31
Completion
2019-02-28

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02724384 on ClinicalTrials.gov