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Efficacy test for evaluating the effect of "composition A" on the skin redness.

Efficacy test for evaluating the effect of "composition A" on the skin redness. - Efficacy test of "composition A" to the skin.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000029583
Enrollment
25
Registered
2017-10-18
Start date
2017-10-18
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

Healthy people

Interventions

Conduct evaluation 1) to 3) with 2 weeks interval. 1)Wash forearm -&gt
3 hours application of 3 different concentration of &quot
composition A&quot
and &quot
placebo&quot
-&gt
evaluation of skin redness induced by ammonia aqueous solution. 2)Wash forearm -&gt
3 hours,3 times,3 days application of 4 different concentration of &quot
. -&gt
evaluation of skin redness induced by ammonia aqueous solution and tape-stripping of stratum corneum. 3)Wash forearm -&gt
3 hours application of 4 different concentration of &quot
tape-stripping of stratum corneum.

Sponsors

Kao Corporation
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1) 20-49 years old healthy man 2) Men who have healthy and non-troubled skin on their forearm

Exclusion criteria

Exclusion criteria: -Man who have dermatitis (atopic dermatitis etc.). -Man under-medication. -Man who have experience of skin troubled with products containing ammonium aqueous solution. -Man who is judged as "not eligible" by investigator. For example, man who have sunburned skin, man who have pigmentation, man who have hairy skin, man who have significant skin contour by his mascule and blood vessel.

Design outcomes

Primary

MeasureTime frame
Skin redness induced by ammonia aqueous solution after 3 days third times consecutive 3 hours application (total 9 hours application in a day) of "composition A" and "placebo"

Secondary

MeasureTime frame
Stratum corneum components related with skin redness induced by ammonia aqueous solution after 3 days application (third times consecutive 3 hours application, total 9 hours application in a day) of "composition A" and "placebo" Skin redness induced by ammonia aqueous solution after 3 hours application of "composition A", "placebo" and "composition B". Amount of "composition A" and "composition B" transferred to skin after 3 hours application of "composition A", "placebo" and "composition B".

Countries

Japan

Contacts

Public ContactMaeko Iwamura

Kao Corporation Biological Science Research

iwamura.maeko@kao.co.jp+81-285-68-7443

Outcome results

None listed

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