NCT00848666

Brief Summary

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.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 28, 2008

Completed
6 months until next milestone

First Posted

Study publicly available on registry

February 20, 2009

Completed
1 month until next milestone

Study Start

First participant enrolled

April 1, 2009

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2010

Completed
Last Updated

February 24, 2009

Status Verified

February 1, 2009

Enrollment Period

1 year

First QC Date

August 28, 2008

Last Update Submit

February 23, 2009

Conditions

Outcome Measures

Primary Outcomes (1)

  • Cure of tinea pedis

    One year

Study Arms (1)

I

EXPERIMENTAL

Patients with tinea pedis

Drug: Topical therapy

Interventions

One time immersion of the feet in a liquid containing water, alcohol, vinegar, benzoic acid and salicylic acid for a total of 30 minutes.

I

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Otherwise healthy patients with laboratory proven tinea pedis

You may not qualify if:

  • Age lower than 18 and higher than 80

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hillel Yaffe Medical Center

Hadera, 38100, Israel

Location

MeSH Terms

Conditions

Tinea Pedis

Interventions

Therapeutics

Condition Hierarchy (Ancestors)

TineaDermatomycosesMycosesBacterial Infections and MycosesInfectionsSkin Diseases, InfectiousFoot DermatosesFoot DiseasesSkin DiseasesSkin and Connective Tissue DiseasesPruritusSkin ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER GOV

Study Record Dates

First Submitted

August 28, 2008

First Posted

February 20, 2009

Study Start

April 1, 2009

Primary Completion

April 1, 2010

Last Updated

February 24, 2009

Record last verified: 2009-02

Locations