Clinical application of autogenous demineralized dentin matrix prepared immediately after extraction for alveolar bone regeneratio
Not Applicable
- Conditions
- ost of alveolar bone
- Registration Number
- JPRN-UMIN000041510
- Lead Sponsor
- Department of Regenerative Oral Surgery, Unit of Translational Medicine, Nagasaki University Graduate School of Biomedical Sciences
- Brief Summary
The clinical application of APDDM prepared immediately after tooth extraction to bone augmentation, taking advantage of the relatively short preparation time due to partial demineralization. APDDM, as introduced in this study, is an efficient, safe, and reasonable bone substitute. Consequently, this material has the potential to become one of the options as a bone substitute in implant dentistry.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Not provided
Exclusion Criteria
a) Patients who had undergone radiation therapy in the oral and maxillofacial region,b) Patients who had undergone other bone grafting in the surgical area, and who had the history of maxillary sinus disease or symptoms were excluded. c) Patients who had uncontrolled systemic disease were also excluded.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method After implantation of the ADDM at 4, 8, 16, and/or 24 weeks, we evaluated the tissue with histology and radiology.
- Secondary Outcome Measures
Name Time Method