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.
Study Type
OBSERVATIONAL
Enrollment
329
spine fusion surgery utilizing any commercially available bone graft substitute(s), autograft or allograft
UCSF
San Francisco, California, United States
St. Joseph's Hospital - Resurgeons Orthopedics
Atlanta, Georgia, United States
Carrollton Orthopedics
Carrollton, Georgia, United States
Evidence of successful radiographic fusion
Time frame: 6 months, 12 months & 24 months
Maintenance or improvement in neurological status, as compared to baseline scores
Time frame: 6 months 12 months & 24 months
Improvement of pain/function in comparison to pre-operative QOL scores
Time frame: 6 months, 12 months & 24 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Bluegrass Orthopedics & Hand Care Research
Lexington, Kentucky, United States
Arthritis & Joint Center - U. Mass. Memorial
Worcester, Massachusetts, United States
PRESSD
Southfield, Michigan, United States
Henry Ford West Bloomfield Hospital
West Bloomfield, Michigan, United States
Montana Neuroscience Institute Foundation
Missoula, Montana, United States
Physicians Research Options Spine Center
Las Vegas, Nevada, United States
Syracuse Orthopedic Specialists
Syracuse, New York, United States
...and 4 more locations