Bone augmentation by octacalcium and collagen composite
Not Applicable
- Conditions
- Missing tooth
- Registration Number
- JPRN-UMIN000015852
- Lead Sponsor
- Tohoku University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 11
Inclusion Criteria
Not provided
Exclusion Criteria
Patient suffering severe hepatopathy, renal disorders, and heart disease who would affect safety evaluation of this trial Patient who has an allergy drug Patient who is pregnant, possibly pregnant, nursing or considering pregnancy Patient who participated other clinical trial program within 3 months prior to the study entry Others, patient who is unfit for the study as determined by the principal investigator or sub-investigators
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Histological analysis, Radiographycal analysis, Safety assessment by clinical examination and adverse event
- Secondary Outcome Measures
Name Time Method