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NCT Number: NCT04194138

Complex Adult Deformity Surgery (CADS)

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Toronto Western, Toronto, Ontario, Canada

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About this study

Specific Aims:

  • 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.

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

  • Develop and validate a standardized, universal complications classification system for spine surgery
  • Evaluate perioperative blood management approaches, transfusion requirements, including variance in thresholds for blood transfusion and associated complications for adult spinal deformity surgery
  • Assess impact of opioid use and pain management on patient cost, complications and outcomes
  • Evaluate optimal opioid and analgesic usage and protocols for standard work development
  • 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
  • Validation of the PROMIS tool for ASD
  • Establish a core set of PROMs for best practice guidelines for ASD
  • Evaluate patient reported outcome variance for ASD according to SRS-Schwab spine deformity type including variance in baseline PROM domains impacted and variance in improvement in PROM domains
  • Evaluate ASD outcomes compared to population norms and investigate/develop appropriate measures of clinically significant improvement
  • Evaluate clinical outcomes stratifying by patient chronological and physiological age
  • Evaluate measures to quantify patient physiological age including patient frailty for ASD and validate a frailty measurement system for ASD
  • Evaluate the role of functional tests in patient's baseline frailty assessment including hand manometer and Edmonton Frail Scale. See appendix, pages 17 & 18 for details.
  • Evaluate the contribution of patient frailty to patient outcomes, cost of care, disability, and complications
  • Evaluate if patient frailty is a static measure or if frailty is a dynamic measure that can be improved through "pre-habilitation" and if the according associations with reductions in frailty correlate with reductions of cost, complications, and improvement in outcomes
  • Evaluate cost variance for ASD surgery according to patient, institution, and geographical region and evaluate the cost effectiveness of surgical intervention for ASD
  • Evaluate incidence of and risk factors for mental health (MH) compromise among ASD patients and establish best practice guidelines for assessing MH for ASD patients
  • Evaluate the association of MH with surgical complications, outcomes, hospital length of stay and cost for ASD surgery
  • Evaluate the association of social health surgical complications, outcomes, hospital length of stay and cost for ASD surgery and risk factors for routine (home) discharge vs. skilled nursing facility (SNF)/rehabilitation facility
  • Broaden the evaluation of the surgically treated ASD patient to maximize evaluation of the entirety of the episode of care to include steps that can be taken prior to surgery including "prehabilitation," pain management, and MH care to improve treatment outcomes, reduce cost, reduce hospital length of stay, reduce non-routing discharge and reduce early and late complications
  • Establish a core set of standard work guidelines to clinically and radiographically evaluate and treat ASD patients and evaluate the utility of standard work to improve outcomes for ASD and formulate best practice guidelines for surgical treatment of ASD
  • Develop predictive analytic algorithms to risk stratify for best/worst outcomes, complications, sentinel events, and economic loss for ASD surgery

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Criteria:

Inclusion criteria

  • Diagnosis of adult congenital, degenerative, idiopathic or iatrogenic spinal deformity
  • Full body EOS radiographic assessment (sagittal and coronal visualization from skull to foot)
  • Complex patients are defined as and meeting any one of the subsequent criteria:
  • Radiographic criteria:
  • PI-LL ≥ 25 degrees
  • TPA ≥ 30 degrees
  • SVA>15cm
  • Thoracic scoliosis ≥ 70 degrees
  • Thoracolumbar/lumbar scoliosis ≥ 50 degrees
  • Global coronal malalignment >7cm
  • Procedural criteria:
  • Posterior spinal fusion > 12 levels
  • 3 column osteotomy or ACR
  • Geriatric criteria:
  • Age >65 years and minimum 7 levels of spinal instrumentation during surgery

Exclusion criteria

  • Age <18 years of age
  • Active spine tumor or infection
  • Deformity due to acute trauma
  • Neuromuscular conditions/diseases (Parkinson's, Multiple Sclerosis, Post-polio syndrome)
  • Syndromic scoliosis
  • Inflammatory arthritis/auto immune diseases (Rheumatoid arthritis, Lupus, Ankylosing Spondylitis)
  • Prisoners
  • Women who are pregnant
  • Non English speaking patients

Treatment and study plan

Index or spine revision surgery for complex adult spinal deformity

Procedure

Surgical interventions will be patient specified by treating surgeon.

Primary outcomes

  1. Scoliosis Research Society (SRS) 22r

    Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up

    Scoliosis specific patient reported outcome

  2. Oswestry Disability Index (ODI)

    Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up

    Spine specific patient reported outcome

  3. Veterans RAND 12 Item Health Survey (VR-12)

    Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up

    Patient reported outcome

  4. Radiographic Evaluation

    Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up

    Cobb angles, Coronal & Sagittal balance, spinopelvic measures

  5. Patient-Reported Outcome Measurement Information System (PROMIS) - Anxiety

    Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up

    Computer adaptive PROs

  6. Patient-Reported Outcome Measurement Information System (PROMIS) - Depression

    Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up

    Computer adaptive PRO

  7. Patient-Reported Outcome Measurement Information System (PROMIS) - Pain Interference

    Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up

    Computer adaptive PRO

  8. Patient-Reported Outcome Measurement Information System (PROMIS) - Physical Function

    Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up

    Computer adaptive PRO

  9. Patient-Reported Outcome Measurement Information System (PROMIS) - Social Role Satisfaction

    Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up

    Computer adaptive PRO

  10. Patient-Reported Outcome Measurement Information System (PROMIS) - Social Satisfaction (DSA)

    Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up

    Computer adaptive PRO

  11. Visual Analog Scale - Back Pain

    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)

  12. Visual Analog Scale - Leg 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)

Secondary outcomes

  1. Edmonton Frail Scale

    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

  2. Canadian Study of Health and Aging (CSHA)

    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

  3. Adverse Events

    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

Study contacts

Contact information is provided by the study sponsor or research team.

Christine Baldus, MS

CONTACT

[email protected]

618-444-4130

Ray Pinteric

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

International Spine Study Group Foundation

Other

Collaborators

  • Globus Medical Inc
  • Medtronic
  • SI-BONE, Inc.

Registry information

Official study title

Multi-Center Prospective Evaluation of Complex Adult Spinal Deformity Surgery

Acronym: CADS

Important dates

Study start
2018
Primary completion
2028
Study completion
2032
First posted
Dec 11, 2019
Registry last updated
Feb 17, 2026

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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