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

OrthoGeorgia

Status: Unknown

Conditions: Lumbar Fusion

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT01833962

001-3708

Details and patient eligibility

About

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.

Enrollment: 100 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

100 participants in 1 patient group

Actifuse

Description:

Patients who recieved Actifuse synthetic bone brafting material