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Clinical Trial Summary

This is an observational, prospective, non-randomised, multi-centred post market clinical follow-up study to compile real world clinical data on safety and efficacy of the synthetic bone graft substitutes in a commercial clinical setting in long bone and extremity defects and in spinal fusion procedures.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03570606
Study type Observational
Source Ceramisys Ltd
Contact Rebecca Hutchinson
Phone +441142327070
Email b.hutchinson@ceramisys.com
Status Recruiting
Phase
Start date June 13, 2019
Completion date June 2026

See also
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