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Safety, Radiological and Patient Reported Outcomes of i-FACTOR+ Matrix Bone Graft Device - A Canadian, Multicenter, Post-Market Clinical Investigation — CAPREG  

Degenerative Disc Disease Clinical Trial

Official title:
Safety, Radiological and Patient Reported Outcomes of i-FACTOR+ Matrix Bone Graft Device - A Canadian, Multicenter, Post-Market Clinical Investigation

Clinical Trial Summary

The study intends tracking the usage patterns of a Bonegraft device within spine surgery in a multicenter setting in Canada.

Clinical Trial Description

The study wil track the usage patterns of a bone graft by identifying and classifying spine surgery procedures by access and segment type within the spins and furthet, record and analyse safety and performance measures associated with each classification. This is a post-market surveillance study ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05144126
Study type Interventional
Source CeraPedics, Inc
Contact Shankar Sivshankar, MS
Phone +447975566265
Email ssivshankar@cerapedics.com
Status Not yet recruiting
Phase N/A
Start date January 2022
Completion date September 2025
View Details
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