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 |
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.
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
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