Examination of effectiveness of combination therapy of periodontal tissue regeneration drug Regroth and bone substitute material for periodontal tissue regeneratio
Not Applicable
- Conditions
- Periodontal Disease
- Registration Number
- JPRN-UMIN000034480
- Lead Sponsor
- Tokushima University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Not provided
Exclusion Criteria
Patients with severe systemic disease Patients who may be pregnant or pregnant Patients with mental illness Patients with hypersensitivity to "Regroth" Patient with malignant tumor in oral cavity or patient with an its history Case of predicted not to able to complete closure of the wound surface when filling with substitute bone material Tooth for severe periodontal disease and tooth extraction adapted tooth
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Increase in new alveolar bone at 9 months after periodontal surgery
- Secondary Outcome Measures
Name Time Method