3 results
Approved WMOCompleted
With this study we aim to determine the feasibility of Smooth Seton placement in patients with perianal fistulas
Approved WMOCompleted
The primary objective of this study is to demonstrate the non-inferiority of AttraX® Putty as a bone graft substitute for autograft in instrumented posterolateral fusion of the thoracolumbar spine, in terms of efficacy and safety.
Approved WMORecruiting
The primary objective is to demonstrate non-inferiority of MagnetOsTM Granules compared to autograft in instrumented posterolateral spinal fusion, in terms of efficacy and safety by means of an intra-patient model.