Pre-market clinical study shows 93% fusion at 12 months 1
A Lazary, PP Varga et al. First-In-Human Study with a Novel Synthetic Bone Graft, OssDsign Catalyst®, in Transforaminal Lumbar Interbody Fusion with Instrumented Posterolateral Fusion. Biomed J Sci & Tech Res 54(4)2024.
Study background
First-in-human study
17 patients
Single level TLIF with Posterolateral Fusion
Study results
93% fusion at 12 months
Improvements in all clinical outcomes at 12 months (VAS, ODI, SF-36, GTO)
No graft related adverse events
Note that the referenced publication describes an investigational clinical study performed in Europe. The use of OssDsign Catalyst described in the publication may not be cleared in all markets. Please refer to your instructions for use for a full list of indications, contraindications, warnings and precautions.
Unprecedented Results in an Uninstrumented Posterolateral Spine Fusion Model 3
Standalone Use in a Trauma Defect Model 8
Total bone formed (dark purple) and remaining graft material (light purple) in a defect filled with standalone OssDsign Catalyst. Data are the mean + SEM (n=5).
Reconstructed µCT images of defects filled with standalone OssDsign Catalyst showing excellent graft incorporation (left) and remodelling (right).
Pre-clinical ovine model demonstrating bone formation away from host bone. SIR2019-10; March 2020 (data on file).
8
Trauma defect pre-clinical lapine model. SIR2019-7; (Sept 2019) and SIR2019-8; April 2020 (data on file).
9
Effects of silicon compounds on biomineralization, osteogenesis, and hard tissue formation. Götz W, et al. Pharmaceutics. 2019 Mar 12;11(3):117.
10
The effect of silicate ions on proliferation, osteogenic differentiation and cell signalling pathways (WNT and SHH) of bone marrow.
*Results from pre-clinical testing may not be predictive of clinical experience in humans. For important safety and intended use information please refer to local IFU.