Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
233 participants
OBSERVATIONAL
2013-12-31
2022-12-31
Brief Summary
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Detailed Description
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Regression analyses will be used to evaluate the association between patient demographics, comorbidities, treatment history, spinal deformity characteristics, surgical characteristics, treatment-related AEs and pre-surgical status to self-reported and radiographic outcomes after surgery.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Elderly suffering of spine deformity
Spinal deformity patients over the age of 60 years undergoing elective surgery and requiring fusion of at least 5 levels.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Diagnosis of adult spinal deformity either in the coronal or sagittal plane requiring at the minimum a 5-level spinal fusion procedure
* Ability to understand the content of the patient information / Informed Consent Form
* Willingness and ability to participate in the clinical investigation according to the Clinical Investigation Plan (CIP)
* Signed and dated Institutional Review Board (IRB)/Ethics Committee (EC)-approved written informed consent
* Reconsent of patients for the 5 year follow-up if required by the IRB/EC
Exclusion Criteria
* Neurodegenerative disease or paralysis
* Unlikely to comply with follow-up
* Institutionalized individuals
* Any not medically managed severe systemic disease
* Recent history (≤ 3 months) of substance abuse (ie, recreational drugs, alcohol) or psychosocial disturbance that would preclude reliable assessment
* Prisoner
* Presence of active malignancy
* Has active, overt bacterial infection, systemic or local
* History of recent(≤ 3 months) fracture/malignancy in the spinal region
* Participation in any other medical device or medicinal product study within the previous month that could influence the results of the present study
60 Years
ALL
No
Sponsors
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AO Innovation Translation Center
OTHER
AO Foundation, AO Spine
OTHER
Responsible Party
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Principal Investigators
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Stephen Lewis, MD
Role: PRINCIPAL_INVESTIGATOR
University of Toronto
Sigurd Berven, MD
Role: PRINCIPAL_INVESTIGATOR
University of California, San Francisco
Locations
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UCSF Medical Center
San Francisco, California, United States
University of Minnesota
Minneapolis, Minnesota, United States
Washington University Orthopedics
St Louis, Missouri, United States
New York Presbyterian - Columbia University Medical Center
New York, New York, United States
University of Virginia
Charlottesville, Virginia, United States
Toronto Western Hospital
Toronto, Ontario, Canada
Queen Mary Hospital
Hong Kong, , China
Nanjing University Medical School
Nanjing, , China
Rigshospitalet
Copenhagen, , Denmark
Hamamatsu University School of Medicine
Hamamatsu, , Japan
St. Maartens Kliniek
Nijmegen, , Netherlands
Hospital Vall d'Hebron
Barcelona, , Spain
Aciboden Maser Hospital
Istanbul, , Turkey (Türkiye)
Countries
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Other Identifiers
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PEEDS
Identifier Type: -
Identifier Source: org_study_id
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