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A clinical trial of the external preparations on the keratosis patients.

A clinical trial of the external preparations on the keratosis patients. - A clinical trial of the external preparations on the keratosis patients.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000023904
Enrollment
30
Registered
2016-09-27
Start date
2016-09-28
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

Keratosis

Interventions

Apply topical prescribed drug for keratosis twice a day for 8 weeks. Apply topical comparator product twice a day for 8 weeks.

Sponsors

Shiba Palace Clinic
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1) Japanese. 2) The persons who have dry and/or stiff feeling in the facial skin. 3) The persons who can peel off the goods for double eyelid at the time. 4) The persons who do not mind the base material and/or solvents adhere to the eyelashes at the time of the replica picking (, if the patients with eyelash extensions). 5) The persons with tending to stay indoors and who have no plans to go out (travel, business trip, etc) during the test period. 6) The persons who agree with the joining this study based on the consent by the document. 7) Patients with some keratosis on the test site (Corner of the eye and lower eyelid) that was diagnosed by the principal investigator or the sub-investigator. 8) Patients who do not have scratches, warts, pimples or burns on the test site, which might have negative impact in the evaluation and measurement. 9) Patients who have wrinkles on the test site, which belongs to the grade 3 to 6 ("Evaluation guidelines for the new efficacy acquisition of Anti-wrinkle product" published by Japanese cosmetic science society). 10) Patients who have the wrinkles belonging to similar grade in the left and right on the test site.

Exclusion criteria

Exclusion criteria: 1) Patients with history of allergy to cosmetics. 2) Patients who are receiving hormone replacement therapy. 3) Patients with experience of cosmetic medicine that might have negative impact on the test site. 4) Patients who are being treated with dermatology. 5) Pregnant or lactating patients. Patients with suspicion of pregnancy. 6) Patients who are participating in other clinical trials 7) Patients deemed inappropriate to participate in this study by the principal investigator or the sub-investigators.

Design outcomes

Primary

MeasureTime frame
Efficacy (keratosis and wrinkle grade) and safety assessment of the test samples by the principal investigator or the sub-investigator before and after the four- and the eight-week application.

Countries

Japan

Contacts

Public ContactMiwa Kaneko

SOUKEN CO., LTD Secretariat

m_kaneko@mail.souken-r.com03-5408-1557

Outcome results

None listed

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