Index or spine revision surgery for complex adult spinal deformity
ProcedureSurgical interventions will be patient specified by treating surgeon.
NCT Number: NCT04194138
Evaluate surgical treatment outcomes and identify best practice guidelines for complex adult spinal deformity (ASD) patients, including radiographic and clinical outcomes, surgical and postoperative complications, risk factors for and revision surgery rates, and the role of standard work to improve patient outcomes and reduce surgical and postoperative complications.
Interested in participating?
Request Info18 year and older
All sexes
Observational
Toronto Western, Toronto, Ontario, Canada
Specific Aims:
a. Complex ASD patients will be defined based upon clinical, radiographic and/or procedural criteria identified in an analysis of the existing ISSG ASD database: i. Magnitude of coronal and/or sagittal spinal deformity ≥75th percentile of patients in the ISSG database.
ii. Clinical or Radiographic parameters that corresponded to patients in the ISSG database that had complications requiring revision spine surgery and/or patients that had hospital length of stay >9 days.
iii. Procedures involving 3 column osteotomies and/or anterior column reconstruction (ACR) of the spine
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Criteria:
Inclusion criteria
Exclusion criteria
Surgical interventions will be patient specified by treating surgeon.
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Scoliosis specific patient reported outcome
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Spine specific patient reported outcome
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Patient reported outcome
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Cobb angles, Coronal & Sagittal balance, spinopelvic measures
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Computer adaptive PROs
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Computer adaptive PRO
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Computer adaptive PRO
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Computer adaptive PRO
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Computer adaptive PRO
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
Computer adaptive PRO
Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up
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
Self-reported leg pain on scale of 0 (No pain) to 10 (severe pain)
Time frame: Change from Preop to 3months and 1, 2, 5 & 10 year follow-up
Evaluate frailty on scale of 0 to 17 where higher scores mean more frail
Time frame: Change from Preop to 3months and 1, 2, 5 & 10 year follow-up
Frailty scale of 1 to 8; higher scores mean more frail
Time frame: 3 months and 1, 2, 5 & 10 year post treatment
Occurrence of Adverse events meeting reporting criteria and their relationship to intervention throughout the study
Contact information is provided by the study sponsor or research team.
International Spine Study Group Foundation
Other
Multi-Center Prospective Evaluation of Complex Adult Spinal Deformity Surgery
Acronym: CADS
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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