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

Status unconfirmed

Conditions studied: Lumbar Fusion

In brief

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.

Key facts

Study ID

NCT01833962

Run by

OrthoGeorgia

People needed

100

Starts

2013-01-01

Expected to finish

2015-12-01

Last updated by the study team

2015-04-21

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 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

You may not qualify if…

• 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

Where it is running

• OrthoGeorgia — Macon, Georgia, United States

Full record on ClinicalTrials.gov

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