Clinical trials for evaluating the effectiveness of a new dental biofilm removing device on palatine mucosa
Not Applicable
- Conditions
- Oral hygiene failure
- Registration Number
- JPRN-UMIN000031232
- Lead Sponsor
- Tohoku University Graduate School of Dentistry
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 5
Inclusion Criteria
Not provided
Exclusion Criteria
(1)Patients who has oral mucosal disease (2)Patinets with severe vomiting reflex (3)Patients who can not stop taking analgesic from the day before pain evaluation (4)Patients who have judged that it is difficlt to participate in this trail
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Removal rate of biofilm on platal mucosa
- Secondary Outcome Measures
Name Time Method 1.Time to remove all biofilm on platal mucosa 2.Cleaning rate(comparison before and after treatment)