A clinical feasibility study to evaluate the effectiviness and safety of VivescOs TM as bone graft for reconstruction of intra-oral osseous defects.
Completed
- Conditions
- Intra-oral defects, due to loss of teeth/molars after trauma or extraction, were reconstructed with VivescOs.
- Registration Number
- NL-OMON24005
- Lead Sponsor
- Isotis, Bilthoven, the Netherlands
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 10
Inclusion Criteria
Repair of the intra-oral defect was indicated as preparation for dental implant placement in a secondary stage.
Exclusion Criteria
1. Presence of local or systemic disease;
2. Pregnancy, cancertherapy;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method