chronOS Implant Evaluation Study. The Canberra Surgicentre and Synthes Australia are conducting a clinical study to evaluate the performance of chronOS granules (bone substitute) following the extraction of wisdom tooth/teeth to prevent the risk of periodontal defects.
Not Applicable
Recruiting
- Conditions
- Mandibular M3 extraction may result in bony periodontal defects on the distal surface of the adjacent second molar.Oral and Gastrointestinal - Inflammatory bowel diseaseDental health.Oral and Gastrointestinal - Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
- Registration Number
- ACTRN12608000092392
- Lead Sponsor
- Canberra Surgicentre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Age >= 18 years
Removal of two mandibular M3
Mesioangular or horizontal M3 position
Agreement for return follow-up for at least 12 months.
Exclusion Criteria
Age < 18 years
No adjacent M2
Diabetic
Chronic steroid use.
Malignant condition
Previous radiotherapy to the maxilla or mandible.
Significant difference between the cementoenamel junction (CEJ) bilaterally, defined as attachment level variance of 1mm or more.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method