The efficacy test of 19220, composite for oral cavity
Not Applicable
- Conditions
- healthy adults
- Registration Number
- JPRN-UMIN000036288
- Lead Sponsor
- Kao Corporation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 10
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 undergoing orthodontic therapy -Subjects with denture -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
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Evaluation of the dental plaque quantity, collection of dental plaque and saliva, photograph of oral cavity, and questionnaire after consecutive 3 days use of 19220 following tooth cleaning
- Secondary Outcome Measures
Name Time Method