Dose escalation trial to evaluate the safety and the efficacy on new bone formation of a single local treatment with lithium carbonate to teeth extraction sockets for dental implant in Japanese participants
Not Applicable
Recruiting
- Conditions
- dental implant
- Registration Number
- JPRN-UMIN000008795
- Lead Sponsor
- Kyushu University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 12
Inclusion Criteria
Not provided
Exclusion Criteria
1 Person who is diagnosed as osteoporosis 2 Person who is suffered from bone disease 3 Person who is not allowed the treatment with lithium carbonate 4 Person who is treated with the medicine which may cause drug interaction with lithium carbonate 5 Body weight<40 kg, >90 kg 6 Person who has a periapical lesion in object tooth 7 Person who has 1- or 2-wall infrabony defects after object tooth extraction 8 Person judged as inappropriate by research contact person
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method