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Efficacy test for oral cavity

The efficacy test of composite 19815 for oral cavity - Efficacy test for oral cavity

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000038298
Enrollment
12
Registered
2019-10-15
Start date
2019-10-15
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 adults

Interventions

Ingest with 19815 composite in 9 times per 3 days. After washout over 4 days, Ingest with positive control1 composite in 9 times per 3 days. After washout over 4 days, Ingest with positive control2 co

Sponsors

Kao Corporation
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: -Male or female of 20 to 59 years of age

Exclusion criteria

Exclusion criteria: -Subjects with systemic illness -Subjects with a disease in the oral cavity and are consulting the medical institution -Subjects undergoing orthodontic therapy -Subjects with denture -Subjects with an implant -The pregnant and subjects who hope to get pregnant during the exam period -Subjects who are taking prescription medicine (except for anti-hay fever) -Subjects deemed inappropriate to participate in this study by the principle investigator

Design outcomes

Primary

MeasureTime frame
Evaluation of the dental plaque quantity, collection of dental plaque and saliva, photograph of oral cavity, and questionnaire after consecutive 2 days use of 19815 following tooth cleaning. Collection of dental plaque, saliva and questionnaire after consecutive 3 days use of 19815.

Countries

Japan

Contacts

Public ContactHatsumi Souno

Kao Corporation Biological Science Research

souno.hatsumi@kao.com+81-285-68-7817

Outcome results

None listed

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