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

OrthoGeorgia100 enrolled

Overview

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.

Study Type

OBSERVATIONAL

Enrollment

100

Conditions

Lumbar Fusion

Eligibility

Sex: ALLMin age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

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

Locations (1)

OrthoGeorgia

Macon, Georgia, United States

Outcomes

Primary Outcomes

Achievement of fusion prior to or at 12 months postoperatively

Time frame: 6 - 12 months year

Data from ClinicalTrials.gov

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