Clinical Trials Directory

Trials / Completed

CompletedNCT00960089

Efficacy Study of LIQUICURE™ to Treat Toe Nail Fungus

Evaluation of the Efficacy of Chesson Labs LIQUICURE™ for Treatment of Onychomycosis

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
63 (actual)
Sponsor
Chesson Laboratory Associates, Inc · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

There is a major clinical need for an inexpensive topically-applied product that can inhibit the growth of the dermatophytes that cause nail fungus. Chesson Labs has developed LIQUICURE with a longer drying/curing time that will allow better nail penetration or adsorption. Though the product may have inherent antimicrobial activity, the product does not contain a drug or antimicrobial agent. Consistent use of LIQUICURE as described will clear fungal nail infection. Clearing of nail fungal infection is defined by negative dermatophyte culture and visual improvement in nail characteristics within six months, with few, if any product-related adverse events.

Conditions

Interventions

TypeNameDescription
DEVICELIQUICURETopical treatment, 1 time/day, 5 days/week

Timeline

Start date
2008-07-01
Primary completion
2010-04-01
Completion
2010-10-01
First posted
2009-08-17
Last updated
2016-01-27

Locations

4 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00960089. Inclusion in this directory is not an endorsement.