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Onychomycosis clinical trials

View clinical trials related to Onychomycosis.

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NCT ID: NCT03098615 Completed - Onychomycosis Clinical Trials

Study Evaluating the Effect of Jublia on Dermatophytomas

Start date: September 2015
Phase: Phase 4
Study type: Interventional

This study will examine how Jublia affects dermatophytomas, which are difficult to treat with other therapeutic options.

NCT ID: NCT03072550 Completed - Clinical trials for Onychomycosis Due to Trichophyton Rubrum

Early Feasibility Study to Evaluate the Efficacy and Safety of the RenewalNailâ„¢ Plasma Treatment System in Patients With Mild to Moderate Onychomycosis (Fungal Nail)

Start date: March 1, 2017
Phase: N/A
Study type: Interventional

Early feasibility study to determine if a three-treatment protocol with the RenewalNailâ„¢ plasma treatment system over a week will result in mycological cure and/or clear nail growth on the treated hallux toe.

NCT ID: NCT03022903 Completed - Clinical trials for Toenail Onychomycosis

Blue Light Photodynamic Therapy Treatment for Distal and Lateral Subungual Toenail Onychomycosis

Start date: September 2015
Phase: N/A
Study type: Interventional

This research study will evaluate the safety and efficacy of using blue light photodynamic therapy (PDT) for treating toenail fungal infections.

NCT ID: NCT02933879 Completed - Onychomycosis Clinical Trials

Randomized, Placebo-Controlled, Double-Blind, Parallel-Group, Multi-Site Phase 2b Clinical Study

Start date: March 21, 2016
Phase: Phase 2
Study type: Interventional

A Randomized, Placebo-Controlled, Double-Blind, Parallel-Group, Multi- Site Phase 2b Clinical Study to Assess the Efficacy, Safety and Tolerability of 8-Week Regimens of NVXT topical product in Patients with Mild to Moderate Onychomycosis

NCT ID: NCT02866032 Completed - Clinical trials for Distal Subungual Onychomycosis

Study to Evaluate the Efficacy and Safety of Topical MOB015B in the Treatment of Mild to Moderate Distal Subungual Onychomycosis (DSO)

Start date: September 2016
Phase: Phase 3
Study type: Interventional

The primary objective of this study is to evaluate the efficacy of topical MOB015B in patients with mild to moderate distal subungual onychomycosis (DSO). The secondary objective is to evaluate the safety of topical MOB015B in patients with mild to moderate DSO.

NCT ID: NCT02859519 Completed - Clinical trials for Distal Subungual Onychomycosis

A Multi-centre, Double-blind, Randomized, Vehicle-controlled Study of Efficacy and Safety of Topical MOB015B in the Treatment of Mild to Moderate Distal Subungual Onychomycosis (DSO)

Start date: October 2016
Phase: Phase 3
Study type: Interventional

The primary objective of this study is to evaluate the efficacy of topical MOB015B in patients with mild to moderate distal subungual onychomycosis (DSO). The secondary objective is to evaluate the safety of topical MOB015B in patients with mild to moderate DSO.

NCT ID: NCT02812771 Completed - Onychomycosis Clinical Trials

Safety and Pharmacokinetics of Efinaconazole Topical Solution in Subjects With Mild to Severe Onychomycosis

Start date: August 4, 2016
Phase: Phase 4
Study type: Interventional

Safety and Pharmacokinetics (PK) of a once daily topical application of efinaconazole in the treatment of pediatric subjects with mild to severe onychomycosis of the toenails.

NCT ID: NCT02812043 Completed - Clinical trials for Non-dermatophyte Onychomycosis

Comparison Between Long-pulsed Nd:YAG, Amorolfine and Combination Treatment in Treating Non-dermatophyte Onychomycosis

Start date: August 2016
Phase: Phase 4
Study type: Interventional

This study aims to compare the efficacy and safety of amorolfine, long-pulsed Nd:YAG laser and the combination between amorolfine and long-pulsed Nd:YAG in treating the non-dermatophyte and mixed-infection onychomycosis.

NCT ID: NCT02798380 Completed - Onychomycosis Clinical Trials

Efficacy, Safety, and Tolerability of HTS-519 Insert in Patients With Toenail Fungus of the Big Toenail

Start date: July 2016
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the efficacy, safety and tolerability of HTS-519 Inserts in the treatment of mild to moderate toenail fungus disease of the big toenail.

NCT ID: NCT02714504 Completed - Onychomycosis Clinical Trials

Anti-mold Azole in the Prophylaxis for Invasive Fusariosis

Fusarproph
Start date: August 2008
Phase: N/A
Study type: Interventional

Patients admitted for autologous or allogeneic hematopoietic cell transplantation, induction-remission chemotherapy for acute myeloid leukemia, myelodysplasia or acute lymphoid leukemia, or to receive immunosuppressive therapy for aplastic anemia will be screened with dermatologic examination. In the presence of any skin lesion in the extremities, direct exam and fungal culture will be performed. If these exams indicate the presence of Fusarium species, patients will receive anti-mold azole prophylaxis