NCT00935870
Completed
Not Applicable
Bioactive Glass (S53P4) as Bone Graft Substitute in Operative Treatment of Depressed Lateral Condyle Fractures, Benign Bone Tumour Cavities and in Spinal Fusion - a 10 Years Follow-up and Bone Density Study.
Vivoxid Ltd1 site in 1 country63 target enrollmentJanuary 2008
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Depressed Lateral Condyle Fracture
- Sponsor
- Vivoxid Ltd
- Enrollment
- 63
- Locations
- 1
- Status
- Completed
- Last Updated
- 16 years ago
Overview
Brief Summary
The main aim is to evaluate the long-term safety and bone healing in the operated area and to compare bioactive glass granules with autogenous bone as a filler material.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Written informed consent obtained; Participation of previous clinical investigation with bioactive glass
Exclusion Criteria
- •The subject is unlikely to adhere to study procedures
- •Concurrent disease or condition that in the opinion of the investigator is contraindicating participation
- •Simultaneous participation in another medical device or investigational drug trial
Outcomes
Primary Outcomes
Not specified
Study Sites (1)
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