Bone Graft Materials Observational Registry



Status:Terminated
Conditions:Cancer, Neurology, Orthopedic, Women's Studies, Hematology
Therapuetic Areas:Hematology, Neurology, Oncology, Orthopedics / Podiatry, Reproductive
Healthy:No
Age Range:18 - Any
Updated:4/6/2017
Start Date:September 2009
End Date:November 2013

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A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice

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.


Inclusion Criteria:

- The patient has failed conservative treatment and is a candidate for spinal fusion
surgery.

- The patient is ≥18 years old and of legal age of consent.

- The patient is, in the investigator's opinion, psychosocially, mentally, and
physically able to fully comply with this protocol, including the post-operative
regimen, required follow-up visits, the filling out of required forms, and have the
ability to understand and give written informed consent.

- The patient is skeletally mature (epiphyses closed).

- The patient has signed the IRB approved informed consent.

- The patient is willing and able to participate in post-operative clinical and
radiographic follow up evaluations for 2 years.

Exclusion Criteria:

- Patient has systemic infection or infection at the surgical site.

- Patient has a medical condition that would interfere with post-operative assessments
and care (i.e., neuromuscular disease, psychiatric disease, paraplegia, quadriplegia,
etc.).

- Patient is in poor general health or any concurrent disease process that would place
the patient in excessive risk to surgery (i.e., significant circulatory or pulmonary
problems, or cardiac disease).

- Patient has a history (present or past) of substance abuse (recreational drugs,
prescription drugs or alcohol) that in the investigator's opinion may interfere with
protocol assessments and/or with the patient's ability to complete the protocol
required follow-up.

- The patient is pregnant/breastfeeding at the time of enrollment, or plans to become
pregnant during the course of the study.

- Patient is participating in another investigational study, which could confound
results.
We found this trial at
13
sites
1635 Divisadero Street
San Francisco, California 94143
2108
mi
from 43215
San Francisco, CA
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436
mi
from 43215
Atlanta, GA
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8 Nagy Jenő utca
Budapest, 1126
4737
mi
from 43215
Budapest,
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150 Clinic Avenue
Carrollton, Georgia 30117
456
mi
from 43215
Carrollton, GA
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1756
mi
from 43215
Las Vegas, NV
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1868 Plaudit Place
Lexington, Kentucky 40509
154
mi
from 43215
Lexington, KY
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1612
mi
from 43215
Missoula, MT
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Nashville, Tennessee 37203
333
mi
from 43215
Nashville, TN
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Plano, Texas 75093
901
mi
from 43215
Plano, TX
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Southfield, Michigan 48072
174
mi
from 43215
Southfield, MI
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Syracuse, New York 13214
417
mi
from 43215
Syracuse, NY
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West Bloomfield, Michigan 48322
178
mi
from 43215
West Bloomfield, MI
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Worcester, Massachusetts 01605
604
mi
from 43215
Worcester, MA
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