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Tinea Pedis clinical trials

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NCT ID: NCT01105013 Not yet recruiting - Tinea Pedis Clinical Trials

Evaluate the Efficacy and Safety of Tolnaftate Cream in the Treatment of Patients With Fungal Infections

Tonaftato
Start date: April 2012
Phase: Phase 3
Study type: Interventional

This is a study clinical, multicenter, Phase III trial, to evaluate the efficacy and safety of tolnaftate cream in the treatment of patients with fungal infections such as Tinea foot, Tinea and Tinea crural body.

NCT ID: NCT01096472 Completed - Tinea Pedis Clinical Trials

Efficacy and Safety of LAS41003 in the Treatment of Inflammatory Tinea Pedis

Start date: February 2010
Phase: Phase 2
Study type: Interventional

The aim of this study is to determine the efficacy and safety of a topical application of the combinational cream LAS41003 compared to application of its mono-substances after once daily treatment in patients with inflammatory tinea pedis.

NCT ID: NCT01013909 Completed - Tinea Pedis Clinical Trials

Comparative Safety and Efficacy Study of New Bifonazol Spray vs Terbinafine Solution vs Placebo

Porsche
Start date: December 2009
Phase: Phase 2
Study type: Interventional

The study shall prove whether 6 consecutive doses of Bifonazole spray show comparable efficacy to a Terbinafine solution applied once.

NCT ID: NCT00893880 Completed - Tinea Pedis Clinical Trials

A Dose Response Trial to Evaluate Clinical and Mycological Effect of Nitric Oxide in Subjects With Tinea Pedis

Start date: June 2009
Phase: Phase 2
Study type: Interventional

A multi-arm trial to evaluate the efficacy and safety of using gaseous nitric oxide to treat moderate to severe tinea pedis.

NCT ID: NCT00869336 Completed - Tinea Pedis Clinical Trials

Multicenter Study of the Efficacy and Safety of Luliconazole Cream in Tinea Pedis (Athlete's Foot)

Start date: March 2009
Phase: Phase 2
Study type: Interventional

To examine the safety and optimal duration of Luliconazole Cream 1% treatments for 14 days or 28 days to achieve "complete clearance" at 2 weeks post treatment.

NCT ID: NCT00856596 Recruiting - Tinea Pedis Clinical Trials

Once a Day Topical Treatment for Athlete's Foot Fungus Inbetween the Toes in Males and Females

Start date: March 2009
Phase: Phase 3
Study type: Interventional

The topical cream, Sertaconazole (Ertaczo), has been FDA approved for the treatment of athlete's foot using twice a day dosing for 4 weeks. This study wants to see if sertaconazole will work equally as well with once a day dosing for 4 weeks for athlete's foot.

NCT ID: NCT00848666 Not yet recruiting - Tinea Pedis Clinical Trials

Safety and Efficacy of a Novel Topical Therapy for Tinea Pedis (Athlete's Foot)

Start date: April 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of a novel topical therapy in patients with laboratory confirmed tinea pedis. During the follow-up period clinical and mycological examinations will be performed.

NCT ID: NCT00835510 Completed - Tinea Pedis Clinical Trials

Clinical Equivalence of Two Butenafine Hydrochloride 1% Creams in Patients With Interdigital Tinea Pedis

Start date: June 2008
Phase: Phase 1
Study type: Interventional

To demonstrate comparable safety and efficacy of Taro Pharmaceuticals Inc. butenafine hydrochloride cream 1% (test product) and Lotrimin Ultra® cream (reference listed drug) in the treatment of interdigital tinea pedis, and to show the superiority of the active treatments over that of the placebo (vehicle).

NCT ID: NCT00804193 Completed - Tinea Pedis Clinical Trials

Safety and Equivalence of a Generic Ciclopirox Olamine Topical Suspension Compared to the Reference Ciclopirox Topical Suspension 0.77% for the Treatment of Tinea Pedis

Start date: June 2004
Phase: N/A
Study type: Interventional

The objectives of this study were to demonstrate comparable safety and efficacy of Ciclopirox Olamine Topical Suspension (Test Product) and Ciclopirox Topical Suspension 0.77% (Reference Product) in the treatment of subjects with tinea pedis, and to show the superiority of the active treatments over that of the vehicle.

NCT ID: NCT00802672 Completed - Tinea Pedis Clinical Trials

Safety and Equivalence of a Generic Ciclopirox Olamine Cream Compared to the Reference Ciclopirox Cream 0.77% for the Treatment of Tinea Pedis

Start date: December 2003
Phase: Phase 3
Study type: Interventional

The objectives of this study were to demonstrate comparable safety and efficacy of Ciclopirox Olamine Cream (Test Product) and Ciclopirox Cream 0.77% (Reference Product) in the treatment of subjects with tinea pedis, and to show the superiority of the active treatments over that of the vehicle.