Clinical research evaluating utility of detection for pathogen of trichophytosis unguium by DERMAQUICK

Clinical research evaluating utility of detection for pathogen of trichophytosis unguium by DERMAQUICK - Evaluating utility of detection for trichophytosis unguium by novel detection kit

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000025907

Enrollment

120

Registered

2017-02-06

Start date

2017-02-13

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

trichophytosis unguium

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Patient who have Suspition of trichophytosis unguium 2) Patient must be at least 20 years of age. Irrespective of sex

Exclusion criteria

Exclusion criteria: 1. 1)Patient who has used Oral antifungal drugs within 6 months 2)Patient who has used antifungal agent for external use within a month prior to enrolling in this study 3)Patient who has difficulty to get informed consent. 4)Patient recognized by investigator as inappropriate for this study

Design outcomes

Primary

Measure	Time frame
To compare efficiency of detection for pathogen of trichophytosis unguium to test samples from suspected area as trichophytosis unguium by DERMAQUICK and by direct microscopy	—

Secondary

Measure	Time frame
Convenience of detection	—

Countries

Japan

Contacts

Public ContactKazuhito Hayashibe

Hayashibe Dermatology Clinic Dermatology

hayashibe@ikkeikai.org079-565-8808

Outcome results