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Trials / Completed

CompletedNCT00771342

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

A Blinded Placebo Controlled Single Cross-over Clinical Trial to Evaluate Fungicidal Activity With Topical Application of 1% Gaseous Nitric Oxide in Subjects With Moderate to Severe Tinea Pedis (Athlete's Foot)

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Nitric BioTherapeutics, Inc · Industry
Sex
All
Age
19 Years
Healthy volunteers
Not accepted

Summary

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

Conditions

Interventions

TypeNameDescription
DRUGNitric Oxide1% gaseous nitric oxide, delivered for 40 minutes daily for 3 consecutive days
DRUGNitrogenNitrogen gas, delivered topically for 40 minutes daily for 3 consecutive days

Timeline

Start date
2008-12-01
Primary completion
2009-06-01
Completion
2009-08-01
First posted
2008-10-13
Last updated
2010-02-03

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT00771342. Inclusion in this directory is not an endorsement.

Efficacy Study to Evaluate the Effect of Nitric Oxide on the Treatment of Tinea Pedis (Athlete's Foot) (NCT00771342) · Clinical Trials Directory