Efficacy test for oral cavity

Not Applicable

• Conditions: healthy adults

• Registration Number: JPRN-UMIN000037517
• Lead Sponsor: Kao Corporation

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-08-01
• Study Completion: 2019-12-31
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up continuing
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

Not provided

Exclusion Criteria

-Subjects with systemic illness -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 full denture -Subjects with mobile tooth -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 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 deemed inappropriate to participate in this study by the principle investigator

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Measurement of oral index. Taking impression and photography of oral cavity. Questionnaire. Each measurements are taken 3 times, before starting test, after using composite19615 for 12 weeks and 24 weeks. Digital dental radiography, before starting test and after using 19615 for 24 weeks.