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Clinical Trial Summary

The main objective is to compare efficacy, in terms of antifungal activity of Loceryl Nail Lacquer associated with a Cosmetic Varnish and Loceryl Nail Lacquer alone, in the treatment of mild to moderate toenail Distal Subungual Onychomycosis. The second objective of this study will be photographic follow-up of clinical improvement and cure after the initial treatment period of 12 weeks, for 15 additional months.


Clinical Trial Description

Study center: A total of 50 subjects were to be included in 1 site in Iceland. Methodology: - Group Loceryl Nail Lacquer+ Cosmetic Varnish: - Loceryl Nail Lacquer to be applied once weekly for 12 weeks on all affected toenails, - Cosmetic varnish to be applied once weekly for 12 weeks on all affected toenails and/or all toenails. - Group Loceryl Nail Lacquer alone: - Loceryl Nail Lacquer to be applied once weekly for 12 weeks on all affected toenails. - All eligible subejct with no clinical sign of clinical aggravation of Onychomycosis at week 12, could continue to apply Loceryl Nail Lacquer alone, once a week for 15 additional months (or less in case of complete cure). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02321098
Study type Interventional
Source Galderma R&D
Contact
Status Completed
Phase Phase 4
Start date February 2014
Completion date January 2016

See also
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Completed NCT04000386 - A Study of Efficacy of Zinc Oxide Nanoparticles Coated Socks in Prevention of Unpleasant Foot Odor N/A
Completed NCT02705664 - Treatment of Onychomycosis With Loceryl (Amorolfine) Nail Lacquer 5% Versus a Two-course Treatment With Urea 40% Ointment and Bifonazole Cream 1% Phase 4