Trials / Completed
CompletedNCT00810043
Medtronic SCORE Study - Study of Curette Use for Obtaining Restoration of Vertebral Body Anatomy in Balloon Kyphoplasty
Study of Curette Use for Obtaining Restoration of Vertebral Body Anatomy in Balloon Kyphoplasty
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 120 (actual)
- Sponsor
- Medtronic Spine LLC · Industry
- Sex
- All
- Age
- 50 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this study is to measure the effect that the scraping and scoring of vertebral cancellous bone using the Kyphon® Curette has on vertebral body anatomy height restoration and angular deformity correction during a balloon kyphoplasty procedure.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Kyphon® Curette | The Kyphon® Curette is intended to scrape and score bone in the spine. It may be used as an adjunctive device with Kyphon's family of standard access and fracture reduction instruments designed to treat compression fracture during balloon kyphoplasty procedures |
Timeline
- Start date
- 2009-02-01
- Primary completion
- 2010-10-01
- Completion
- 2010-10-01
- First posted
- 2008-12-17
- Last updated
- 2017-12-08
- Results posted
- 2011-11-30
Locations
13 sites across 3 countries: United States, Belgium, Germany
Source: ClinicalTrials.gov record NCT00810043. Inclusion in this directory is not an endorsement.