Prospective Evaluation of Elderly Deformity Surgery
Status: | Active, not recruiting |
---|---|
Conditions: | Women's Studies |
Therapuetic Areas: | Reproductive |
Healthy: | No |
Age Range: | 60 - Any |
Updated: | 12/27/2018 |
Start Date: | December 2013 |
End Date: | December 2022 |
Prospective Evaluation of Elderly Deformity Surgery: A Prospective Observational, Multicenter Study
As the population continues to age, the prevalence of spinal deformity surgery for older
patients is increasing. Questions regarding the suitability of these patients to undergo
large spinal procedures and whether the outcomes merit the risks involved are not well known.
patients is increasing. Questions regarding the suitability of these patients to undergo
large spinal procedures and whether the outcomes merit the risks involved are not well known.
225 subjects greater than or equal 60 years of age with moderate and severe adult spinal
deformity requiring surgical correction will be enrolled in a prospective multicenter
international study. Spinal deformity will be defined as any coronal or sagittal plane spinal
deformity in patients who have not undergone any previous spinal surgery (with the exception
of prior decompression of a maximum of 2 levels) necessitating at a minimum a 5-level spinal
fusion procedure. Standard radiographs and cross sectional imaging will be performed
preoperatively, postoperatively, at 24 months and 5 years after surgery. Preoperative disease
specific and general health questionnaires will be completed by all patients (EQ-5D, ODI,
SRS-22r, NRS for back and leg pain). Follow up visits with questionnaires will be performed
at 10 weeks (± 6 weeks), 12 months (± 2 months), 24 months (± 2 months) and 5 years (±6
months) post-operatively. All treatment-related AEs will be documented.
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.
deformity requiring surgical correction will be enrolled in a prospective multicenter
international study. Spinal deformity will be defined as any coronal or sagittal plane spinal
deformity in patients who have not undergone any previous spinal surgery (with the exception
of prior decompression of a maximum of 2 levels) necessitating at a minimum a 5-level spinal
fusion procedure. Standard radiographs and cross sectional imaging will be performed
preoperatively, postoperatively, at 24 months and 5 years after surgery. Preoperative disease
specific and general health questionnaires will be completed by all patients (EQ-5D, ODI,
SRS-22r, NRS for back and leg pain). Follow up visits with questionnaires will be performed
at 10 weeks (± 6 weeks), 12 months (± 2 months), 24 months (± 2 months) and 5 years (±6
months) post-operatively. All treatment-related AEs will be documented.
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.
Inclusion Criteria:
- Age 60 years or older at the time of surgery
- 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:
- Any previous spinal procedure (except prior decompression of a maximum of 2 levels)
- 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
We found this trial at
6
sites
New York, New York 10065
Principal Investigator: Lawrence G Lenke, MD
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Minneapolis, Minnesota 55455
(612) 625-5000
Principal Investigator: Robert Morgan, MD
Univ of Minnesota With a flagship campus in the heart of the Twin Cities, and...
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Charlottesville, Virginia 22903
(434) 924-0311
Principal Investigator: Christopher Shaffrey, MD
University of Virginia The University of Virginia is distinctive among institutions of higher education. Founded...
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