The efficacy test of BOC777, composite for oral cavity
Not Applicable
- Conditions
- Healthy adults
- Registration Number
- JPRN-UMIN000024068
- Lead Sponsor
- Kao Corporation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 60
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 the orthodontic therapy -Subjects with denture -The pregnant and subjects who hope to get pregnant during the exam period -Subjects who are taking prescription medicine -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 Collection of saliva, tongue plaque and dental plaque and measurement of oral index and questionnaire each of the 4 times, before starting test, after using BOC 777 for 2 weeks and 8 weeks and in 2 weeks after finishing using BOC 777.
- Secondary Outcome Measures
Name Time Method