Skip to content

The exploratory study on usability of topical antifungal drugs.

The exploratory study on usability of topical antifungal drugs. - The exploratory study on usability of topical antifungal drugs.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000031817
Enrollment
40
Registered
2018-03-28
Start date
2018-03-28
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

Adults

Interventions

Luconac solution 5% is applied to all toes. Single dose. Clenafin solution 10% is applied to all toes. Single dose.

Sponsors

Medical Corporation Shinanokai Samoncho Clinic
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Adult male and female with healthy toes. 2.Those who have not medicated with topical antifungal drugs. 3.Those who have toes without inflammatory and external injury including nail trinea.

Exclusion criteria

Exclusion criteria: 1.Those who have malfunctions on fingers or upper limb that impede the embrocation action. 2.Those who have other diseases that may impede the embrocation action, such as visual handicapped except hypermetropia or neuropathy etc. 3.Those who have diseases that impede the informed concent or the operation of study, such as dementia. 4.Those who are during lactation, pregnancy or possible pregnancy. 5.Those who have history of hypersensitiveness on the study drugs. 6.Others who are deemed inappropriate by the investigator to conduct this study.

Design outcomes

Primary

MeasureTime frame
VAS of five assessements on the usability.

Countries

Japan

Contacts

Public ContactSatoko Shimizu

Tokyo Research Center of Clinical Pharmacology Co., Ltd. Clinical trial promotion II dept.

s-shimizu@trcp.co.jp03-5366-3454

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026