A Retrospective Study of Actifuse Synthetic Bone Graft Versus Other Bone Graft Substitutes in Patients Requiring Lumbar Fusion

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01833962

Enrollment

100

Registered

2013-04-17

Start date

2013-01-31

Completion date

2015-12-31

Last updated

2015-04-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lumbar Fusion

Keywords

Lumbar fusion rates, Actifuse synthetic bone graft, Baxter Healthcare, Other synthetic bone graft

Brief summary

The purpose of this study is to assess fusion status in patients who underwent spinal fusion with Actifuse synthetic bone graft versus other bone graft material (including autograft) in achieving lumbar spinal fusion.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

* Any patient 18 years of age or older * Patients with a minimum follow up of 1 year * Patients who have previously undergone TLIF, PLIF,PLF, XLIF procedures

Exclusion criteria

* Patients under the age of 18 * Any patient with less than 1 year of follow up history at the time of first data analysis * Any patient that the primary investigator deems as an unfit candidate

Design outcomes

Primary

Measure	Time frame
Achievement of fusion prior to or at 12 months postoperatively	6 - 12 months year

Countries

United States

Outcome results