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Tinea Pedis clinical trials

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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: 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.

NCT ID: NCT00781664 Completed - Tinea Pedis Clinical Trials

Cumulative Irritation Test

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

The purpose of this study is to determine the cumulative irritation potential of the products listed by the Sponsor.

NCT ID: NCT00771342 Completed - Tinea Clinical Trials

Efficacy Study to Evaluate the Effect of Nitric Oxide on the Treatment of Tinea Pedis (Athlete's Foot)

Start date: December 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the fungicidal efficacy of nitric oxide and it's effect on the clinical signs and symptoms associated with Tinea Pedis

NCT ID: NCT00768599 Completed - Tinea Pedis Clinical Trials

A Study of Econazole Foam 1% in Athlete's Foot

Start date: March 2008
Phase: Phase 2
Study type: Interventional

This is a 6-week clinical study (4 weeks of treatment, once per day, plus a 2-week follow-up period) of a topical foam to treat athlete's foot. The active ingredient in the foam -- econazole nitrate 1% -- is the same active pharmaceutical ingredient in a cream that your doctor can currently prescribe to treat athlete's foot. This study will help to understand if the foam works the same as the cream to treat athlete's foot.

NCT ID: NCT00750139 Completed - Tinea Pedis Clinical Trials

Multicenter Study of the Safety and Efficacy of NAFT-500 in Tinea Pedis

Start date: August 2008
Phase: Phase 3
Study type: Interventional

A research study to compare the safety and effectiveness of an investigational medication called NAFT-500 to placebo, when used in subjects with tinea pedis (athlete's foot).