Trials / Terminated
TerminatedNCT00974623
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
- Status
- Terminated
- Phase
- —
- Study type
- Observational
- Enrollment
- 329 (actual)
- Sponsor
- Baxter Healthcare Corporation · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
A multi-center, prospective, observational patient registry to collect information on the clinical outcomes and "real world" use of approved and commercially available bone graft substitutes, autograft and allograft.
Conditions
- Degenerative Disc Disease
- Herniated Disc
- Spinal Stenosis
- Spondylolithesis
- Spinal Deformity
- Cervical Myelopathy
- Failed Back Surgery Syndrome
- Spinal Cord Neoplasms
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Bone graft substitute, autograft or allograft | spine fusion surgery utilizing any commercially available bone graft substitute(s), autograft or allograft |
Timeline
- Start date
- 2009-09-01
- Primary completion
- 2013-01-01
- Completion
- 2013-11-01
- First posted
- 2009-09-10
- Last updated
- 2017-04-05
Locations
14 sites across 3 countries: United States, Hungary, Netherlands
Source: ClinicalTrials.gov record NCT00974623. Inclusion in this directory is not an endorsement.