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Onychomycosis clinical trials

View clinical trials related to Onychomycosis.

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NCT ID: NCT00443820 Completed - Onychomycosis Clinical Trials

Efficacy Safety, and Tolerability of Topical Terbinafine in Patients With Mild to Moderate Toenail Fungus of the Big Toenail

Start date: December 2006
Phase: Phase 3
Study type: Interventional

This study is designed to assess the efficacy, safety and tolerability of a topical formulation of terbinafine solution applied daily in patients with toenail fungus. This trial will study patients with mild to moderate toenail fungus disease of the big toenail and their responses to two treatment durations, 24 or 48 weeks.

NCT ID: NCT00385502 Completed - Onychomycosis Clinical Trials

A Trial of the Safety and Efficacy of EcoNailâ„¢ in the Treatment of Fungus Infections of the Great Toenail

Start date: September 2006
Phase: Phase 2
Study type: Interventional

Approximately 40 qualified subjects with mild-to-moderate great toenail fungus infection will be treated for 48 weeks with lacquer application to at least one affected great toenail. All subjects will receive treatment with EcoNailâ„¢ lacquer.

NCT ID: NCT00356915 Completed - Clinical trials for Onychomycosis, Toenail Onychomychosis, Toenail Fungus.

Itraconazole Tablets Vs. Itraconazole Capsules vs. Placebo in Onychomycosis of the Toenail.

Start date: July 2006
Phase: Phase 3
Study type: Interventional

Onychomycosis is a common condition accounting for approximately half of all nail disorders. It is most commonly caused by dermatophytes. Itraconazole has been approved for the treatment of onychomycosis in the United States with an approved dosage regimen for the treatment of onychomycosis of the toenail of once daily (QD) treatment with 200mg of itraconazole (two 100 mg capsules) for 12 weeks. Barrier Therapeutics has developed a 200 mg tablet which could be used in a more convenient one-tablet-per-day dosing regimen. This clinical trial will compare the efficacy and safety of this new tablet formulation with itraconazole capsules and placebo.

NCT ID: NCT00253305 Completed - Onychomycosis Clinical Trials

Topical Gel Anti-Fungal Agent for Tinea Unguium

Start date: September 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to compare, in a controlled fashion, the response to two anti-fungal agents, naftifine or terbinafine, with vehicle in novel topical gel formulations in the treatment of subjects with distal subungual tinea unguium of the toenails (onychomycosis). The formulation used as the vehicle for the active agents has been shown in earlier studies to facilitate the penetration of the active agent through fungally-infected nails. This study will examine dose-response and agent differences in terms of efficacy and safety. Once the subject has qualified for the study, he/she will be randomly assigned to one of five study groups, dispensed appropriate study medication and instructed to apply one drop to the great toe designated for study.

NCT ID: NCT00233493 Recruiting - Onychomycosis Clinical Trials

Spread of Dermatophytes Among Families

Start date: March 2005
Phase: N/A
Study type: Observational

The objective is to demonstrate person-to-person spread of dermatophytes of the skin and nails among family members, as measured by fungal culture and DNA typing of the dermatophytes isolated.