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Clinical Evaluation of the Efficacy of a Medical Device in Treatment of Toenail Onychomycosis

NCT03289871 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 112

Last updated 2017-09-21

No results posted yet for this study

Summary

This study evaluates the effect of the medical device "Excilor® Fungal Nail Infection" in the treatment of toenail onychomycosis. Half of the participants will receive the tested product and the other half will receive a comparator (Amorolfin 5%). Patients will be followed during 6 months.

Conditions

  • Onychomycosis

Interventions

DEVICE

Excilor

DRUG

Loceryl 5%

Sponsors & Collaborators

  • Oystershell NV

    lead INDUSTRY

Principal Investigators

  • Nejib Doss, MD · Principal Instruction military hospital of Tunis

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-01-31
Primary Completion
2015-11-30
Completion
2015-11-30

Countries

  • Tunisia

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 NCT03289871 on ClinicalTrials.gov