Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Discontinued due to a strategic shift in research focus. The steering committee decided to replace the broad registry with multiple targeted prospective cohort studies to ensure higher statistical significance and more focused clinical evidence.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| AO Foundation, AO Spine | OTHER |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Details regarding the degenerative spine disorders will be collected with a specific focus on the use of osteobiologics in treating degenerative conditions and their impact on fusion, as well as patient-reported outcomes for these conditions.
The registry is designed to be open-ended. However, a statistical evaluation of the content und structure of database and CRFs in order to investigate the feasibility and quality of data collection is planned to take place prior to the registry expansion.
Variables applicable to patients with a degenerative spine disorder which will be collected in the registry include:
Feasibility phase:
The statistical evaluation of the feasibility and quality of data collection will be performed after the first 5 sites have each enrolled 12 patients with a degenerative pathology and documented one follow-up visit. During this evaluation, enrolment of further patients can be continued.
Based on the findings of this feasibility phase, adjustments to the existing database can be performed before the registry is rolled out on larger scale.
Registry expansion:
Following the evaluation process of the feasibility phase, the registry will be expanded to allow data entry in more sites globally. Multi-site participation of this registry will be rolled-out in stages, and will be offered to sites with appropriate expertise which are selected based on their potential (interest, resources and expected patient volume).
Not provided
Not provided
Not provided
Not provided
| Measure | Description | Time Frame |
|---|---|---|
| Use of Osteobiologics - Within the registry information on the use of osteobiologis (autografts, allografts, BMA/cells, BMP, DBM, matrices/carriers, platelets) are collected | Osteobiologics are classified as autogenous bone graft substitutes, extenders, or enhancers. Types of osteobiologics include demineralized bone matrices (DBM), allografts and allograft formulations, synthetic bone grafts, bone morphogenic proteins, bone marrow aspirate systems, stem cells and platelet-rich plasma systems. The biologics are generally defined as being derived from or replicating natural substances. The osteobiologics are defined as such by possessing one or more of the following properties: osteoinductivity, osteoconductivity, and osteogenicity. Although biologics are classically defined as being derived from or replicating natural substances, a broader definition of an osteobiologic includes synthetic derivatives that may not replicate natural substances, but serve as a bone graft substitute, extender or enhancer. There is not yet defined how the data will be analysed. Data collected can help drive hypotheses and might help to answer unforeseen questions over time. | Every standard of care scheduled follow-up visit up to 3 years |
| Measure | Description | Time Frame |
|---|---|---|
| Neck, Arm, Back, Leg, Thoracic pain Numeric Rating Scale (NRS) | Every standard of care scheduled follow-up visit up to 3 years | |
| Neck Disability Index (NDI) | Every standard of care scheduled follow-up visit up to 3 years |
| Measure | Description | Time Frame |
|---|---|---|
| Information on postoperative adverse events | Data will be entered in the database but there is not yet defined how the data will be analysed. Data collected can help drive hypotheses and might help to answer unforeseen questions over time. | Every standard of care scheduled follow-up visit up to 3 years |
| Duration of postoperative adverse event |
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Patients with a degenerative spine disorder
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Tim Yoon, MD | Principal Coordinating Investigator | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| USC Spine Center, Keck Medical Center of USC | Los Angeles | California | United States | |||
| Emory University School of Medicine |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D019636 | Neurodegenerative Diseases |
| ID | Term |
|---|---|
| D009422 | Nervous System Diseases |
Not provided
Not provided
Not provided
Not provided
Not provided
| Oswestry Disability Index (ODI) | Every standard of care scheduled follow-up visit up to 3 years |
| Euroqol EQ-5D-3L | Every standard of care scheduled follow-up visit up to 3 years |
| Short Form (SF)-36 V2 | Every standard of care scheduled follow-up visit up to 3 years |
| Modified Zung Depression Index | Every standard of care scheduled follow-up visit up to 3 years |
| Distress and Risk Assessment Method (DRAM) | Every standard of care scheduled follow-up visit up to 3 years |
| Scoliosis Research Society (SRS)-22 Questionnaire | Every standard of care scheduled follow-up visit up to 3 years |
| Modified Japanese Orthopedic Association Score (mJOA) | Every standard of care scheduled follow-up visit up to 3 years |
| Type of fusion that was performed (posterior and/or anterior/interbody fusion) | Data will be entered in the database but there is not yet defined how the data will be analysed. Data collected can help drive hypotheses and might help to answer unforeseen questions over time. | 6 months after surgery, if this time point is collected as per standard of care |
| Type of fusion that was performed (posterior and/or anterior/interbody fusion) | Data will be entered in the database but there is not yet defined how the data will be analysed. Data collected can help drive hypotheses and might help to answer unforeseen questions over time. | 12 months after surgery, if this time point is collected as per standard of care |
| Fusion: Bridging trabecular bone across the segment, bone graft resorption, implant subsidence/migration, fatigue failure of spinal instrumentation, radioluciencies around screws, instability on flexion/extension views | Radiological source for interpretation (Clinical assessment, radiographs, CT, MRI, bone scan, other) Data will be entered in the database but there is not yet defined how the data will be analysed. Data collected can help drive hypotheses and might help to answer unforeseen questions over time. | 6 months after surgery, if this time point is collected as per standard of care |
| Fusion: Bridging trabecular bone across the segment, bone graft resorption, implant subsidence/migration, fatigue failure of spinal instrumentation, radioluciencies around screws, instability on flexion/extension views | Radiological source for interpretation (Clinical assessment, radiographs, CT, MRI, bone scan, other) Data will be entered in the database but there is not yet defined how the data will be analysed. Data collected can help drive hypotheses and might help to answer unforeseen questions over time. | 12 months after surgery, if this time point is collected as per standard of care |
| Success of fusion | Data will be entered in the database but there is not yet defined how the data will be analysed. Data collected can help drive hypotheses and might help to answer unforeseen questions over time. | 6 months after surgery, if this time point is collected as per standard of care |
| Success of fusion | Data will be entered in the database but there is not yet defined how the data will be analysed. Data collected can help drive hypotheses and might help to answer unforeseen questions over time. | 12 months after surgery, if this time point is collected as per standard of care |
Data will be entered in the database but there is not yet defined how the data will be analysed. Data collected can help drive hypotheses and might help to answer unforeseen questions over time. |
| Every standard of care scheduled follow-up visit up to 3 years |
| Atlanta |
| Georgia |
| United States |
| The Johns Hopkins University | Baltimore | Maryland | 21287 | United States |
| Mount Sinai Hospital | New York | New York | 10029 | United States |
| New York Presbyterian - Columbia University Medical Center | New York | New York | 10032 | United States |
| BG-Clinic Bergmannstrost | Halle | 06112 | Germany |
| Istituto Ortopedico Rizzoli | Bologna | Bologna | 40136 | Italy |