Exploratory trial to evaluate safety and efficacy of hydroxyapatite film formed by new dental treatment system for caries, dentin hypersensitivity or discolored tooth (investigator-initiated clinical trial)
Not Applicable
- Conditions
- caries, dentin hypersensitivity or discolored tooth
- Registration Number
- JPRN-UMIN000015439
- 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
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
1. Patients who have oral mucosal diseases 2. Past medical history about adverse effects of local anesthetic 3. Pregnancy or possibility of pregnancy 4. Participants of other clinical trial 5. Taking painkillers 6. Patients who are judged as in adequate for this trial by the investigators
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method