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Evaluation test for oral cavity

Evaluation test of composition 220315 for oral cavity - Evaluation test for oral cavity

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000047535
Enrollment
60
Registered
2022-05-10
Start date
2022-06-08
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

Rinsing oral cavity with mouthwash1 for 30 seconds 3 times a day for 8 weeks. Rinsing oral cavity with mouthwash2 for 30 seconds 3 times a day for 8 weeks. Rinsing oral cavity with mouthwash3 for 30 s

Sponsors

Kao Corporation
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: -Male or female of 30 to 59 years of age -Subjects who can come to the test site by their own -Subjects who can sign by their own will -1or2or3 1.Subjects who may bleed from gingival. 2.Subjects with occasional swelling of gingival. 3.Subjects have been diagnosed with swollen gingival or deep periodontal pockets. -Subjects who have 20 or more of their own teeth.

Exclusion criteria

Exclusion criteria: -Subjects with systemic illness. -Subjects who are taking prescription medicine (except for anti-hay fever). -Subjects with a disease in the oral cavity and are consulting the medical institution. -Subjects with periodontal disease is treated -Subjects with the orthodontic therapy. -Subjects with mobile tooth. -Subjects with full denture -Subjects with an implant -Subjects who have regular dental checkups at least 2 times a year. -Subjects who have been prescribed antibiotics for swollen gingival within a year. -The pregnant and subjects who hope to get pregnant during the exam period. -Subjects who usually use gargle. -Subjects with disease in nose -Subjects who dislike perfume, or other odor substances -Subjects who are hypersensitive to chemicals -Subjects with smoking habit -Subjects from outside the company who work in an advertising agency, an investigation, consultancy, mass communication, and the manufacturing industry of health food, cosmetics, toiletries, a sanitary items, and a distributive trade. -Subjects who participate in the other examinations. -Subjects who had health problems (fever, cold-like symptom, abnormal taste or smell, etc.) within 2 weeks prior to the test, or subjects who had a family member living with them who showed abnormalities. -Subjects who had close contact with COVID-19 infected individuals within 2 weeks prior to the study. -Subjects who are confirmed positive in the COVID-19 antigen test on the day of measurement. -Subjects deemed inappropriate to participate in this study by the principle investigator.

Design outcomes

Primary

MeasureTime frame
Measurement of oral index. Measurements are taken 4 times, before starting test, after using mouthwash for 4 weeks and 8 weeks, and 4 weeks after end of intervention.

Secondary

MeasureTime frame
Intraoral photography, questionnaire and saliva collection are taken 4 times, before starting test, after using mouthwash for 4 weeks and 8 weeks, and 4weeks after end of intervention. Halitosis related measurements, collection of plaque and oral gas are taken 2 times, before starting test and after using mouthwash for 8weeks.

Countries

Japan

Contacts

Public ContactHatsumi Souno

Kao Corporation Biological Science Research

souno.hatsumi@kao.com+81-70-4356-2759

Outcome results

None listed

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