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Clinical trial

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.

NCT00935870 is registered in ClinicalTrials.gov with Vivoxid Ltd as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
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.
Lead sponsor
Vivoxid Ltd
Phase
Observational
Overall status
Completed
Start date
January 31, 2008
Completion date
February 28, 2009
Enrollment
63 (actual)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

benign bone tumour cavity, depressed lateral condyle fracture, spinal fusion