Trials / Completed
CompletedNCT01220505
Post Market Surveillance to Evaluate the Effectiveness the Polaris Deformity Spinal System
A Post Market Surveillance Validation to Evaluate the Effectiveness of the Following System: Polaris Deformity Spinal System
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 66 (actual)
- Sponsor
- Zimmer Biomet · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
The purpose of this Post Market Surveillance Validation is to document the performance and clinical outcomes of the Polaris Deformity Spinal System \& Trivium 3D Spinal Deformity Correction System.
Detailed description
The purpose of this Post Market Surveillance Validation is to document the performance and clinical outcomes of the Polaris Deformity Spinal System \& Trivium 3D Spinal Deformity Correction System. We have extended the study tol collect further outcomes data at the 12 month time point.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Surgery | All subjects will have spinal surgery between the levels of T1 and Ilium using the Polaris Deformity Spinal System |
Timeline
- Start date
- 2010-09-01
- Primary completion
- 2014-01-01
- Completion
- 2014-01-01
- First posted
- 2010-10-14
- Last updated
- 2019-12-19
Locations
6 sites across 2 countries: United States, Puerto Rico
Source: ClinicalTrials.gov record NCT01220505. Inclusion in this directory is not an endorsement.