Trials / Unknown
UnknownNCT05144126
Safety, Radiological and Patient Reported Outcomes of i-FACTOR+ Matrix Bone Graft Device - A Canadian, Multicenter, Post-Market Clinical Investigation
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 300 (estimated)
- Sponsor
- CeraPedics, Inc · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The study intends tracking the usage patterns of a Bonegraft device within spine surgery in a multicenter setting in Canada.
Detailed 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
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | CT radioraphic assessment | CT radioraphic assessment |
Timeline
- Start date
- 2022-01-01
- Primary completion
- 2024-05-01
- Completion
- 2025-09-01
- First posted
- 2021-12-03
- Last updated
- 2021-12-03
Source: ClinicalTrials.gov record NCT05144126. Inclusion in this directory is not an endorsement.