Trials / Terminated
TerminatedNCT01528072
Dynesys Spinal System Post Market 522 Study
Post Market Surveillance for the Dynesys Spinal System, Assessing Safety and Fusion.
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 153 (actual)
- Sponsor
- Zimmer Biomet · Industry
- Sex
- All
- Age
- 20 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to assess the safety and fusion rates following posterior lateral fusion with the Dynesys Spinal System used as an adjunct to fusion and compare to literature control.
Detailed description
Study is meant to assess the safety and fusion rates following posterior lateral fusion with the Dynesys Spinal System.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Dynesys Spinal System | Dynesys Spinal System will be used for all subjects |
Timeline
- Start date
- 2012-03-01
- Primary completion
- 2017-04-01
- Completion
- 2017-04-01
- First posted
- 2012-02-07
- Last updated
- 2020-01-29
- Results posted
- 2020-01-29
Locations
9 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT01528072. Inclusion in this directory is not an endorsement.