An observational study in Adult Spinal Deformity, Scoliosis and Kyphosis, sponsored by International Spine Study Group Foundation. Recruiting at 9 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-02-17.
Sponsored by International Spine Study Group Foundation · Observational
Prospective, Multicenter, Case-Control Analysis of the VersaTie Posterior Fixation System to Prevent Proximal Junctional Failure in Long Posterior Spinal Fusion Constructs for Adult Patients
Specific Aims:
Evaluate clinical outcomes utilizing legacy patient reported outcome measures (PROMs) including modified Oswestry Disability Index (mODI), Scoliosis Research Society Questionnaire 22r (SRS-22r), Veterans RAND-12 (VR-12), and numeric pain rating scale (NRS) and compare the results of these legacy PROMs to outcomes scores as measured by the NIH Patient Reported Outcomes Measurement Information System (PROMIS) - PROMIS Anxiety, Depression, Pain Interference, Physical Function, and Social Satisfaction. Secondary aims for PROM research for this study include
660 studies on the registry are indexed under Scoliosis; 186 are open to participants now.
This study's planned enrollment of 225 is above the median of 84 across 256 observational studies indexed under Scoliosis.
Browse Scoliosis studies →International Spine Study Group Foundation is the lead sponsor of 7 studies on the registry; 4 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Multicenter, prospective, observational, study evaluating the safety and performance of the VersaTie System by comparing adult patients receiving minimum 5 level posterior spinal fusion with pedicle screw fixation supplemented at the proximal aspect of the construct with the VersaTie System
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Procedure: Index or revision spine surgery for complex adult spinal deformity
Adult patients receiving minimum 5 level posterior spinal fusion with pedicle screw fixation supplemented at the proximal aspect of the construct with the VersaTie System.
Also known as: VersaTie System
Scoliosis Research Society (SRS) 22r
Scoliosis specific patient reported outcome
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Oswestry
Spine specific patient reported outcome
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Veterans RAND 12 Item Health Survey (VR-12)
Patient reported outcome
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Patient-Reported Outcome Measurement Information System (PROMIS) - Anxiety
Patient reported outcome
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Patient-Reported Outcome Measurement Information System (PROMIS) - Depression
Patient reported outcome
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Patient-Reported Outcome Measurement Information System (PROMIS) - Pain Interference
Patient reported outcome
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Patient-Reported Outcome Measurement Information System (PROMIS) - Physical Function
Patient reported outcome
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Patient-Reported Outcome Measurement Information System (PROMIS) - Social Satisfaction
Patient reported outcome
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Patient-Reported Outcome Measurement Information System (PROMIS) - Social Role
Patient reported outcome
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Visual Analog Scale - Back Pain
Self-reported back pain on scale of 0 (No pain) to 10 (severe pain)
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Visual Analog Scale - Leg Pain
Self-reported leg pain on scale of 0 (No pain) to 10 (severe pain)
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Edmonton Frail Scale
Evaluate frailty on scale of 0 to 17 where higher scores mean more frail
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Canadian Study of Health and Aging (CSHA)
Frailty scale of 1 to 9; higher scores mean more frail
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Adverse Events
Occurrence of Adverse events meeting reporting criteria and their relationship to intervention throughout the study \[Time Frame: 3 months and 1, 2, 5 \& 10 year post treatment\]
Time frame: 3 months and 1, 2, 5 & 10 year post treatment
Not enrolling at this site.
Plan to share: No
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International Spine Study Group Foundation