Trials / Completed
CompletedNCT04984213
Study of the Long-Term Outcomes of Posterior Spinal Fixation With the Karma Device
CORTI-FIX: Clinical and Radiographic Outcomes Following Lumbar Interbody Placement With Posterior Minimally Invasive Intra-Laminar PEEK Ratcheting Fixation Device
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 20 (actual)
- Sponsor
- Spinal Elements · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The primary objective of this clinical study is to measure fusion rate in patients at 12 months following lumbar fusion in combination with posterior fixation using the Karma® device.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Karma Posterior Fixation Device | Posterior Fixation |
Timeline
- Start date
- 2021-08-15
- Primary completion
- 2025-06-16
- Completion
- 2025-06-16
- First posted
- 2021-07-30
- Last updated
- 2025-06-29
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT04984213. Inclusion in this directory is not an endorsement.