Complex Adult Deformity Surgery (CADS)

Study Purpose

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.

Recruitment Criteria

Accepts Healthy Volunteers

Healthy volunteers are participants who do not have a disease or condition, or related conditions or symptoms

No
Study Type

An interventional clinical study is where participants are assigned to receive one or more interventions (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.


An observational clinical study is where participants identified as belonging to study groups are assessed for biomedical or health outcomes.


Searching Both is inclusive of interventional and observational studies.

Observational [Patient Registry]
Eligible Ages 18 Years and Over
Gender All
More Inclusion & Exclusion Criteria

Criteria:

Inclusion Criteria:

1. Diagnosis of adult congenital, degenerative, idiopathic or iatrogenic spinal deformity. 2. Full body EOS radiographic assessment (sagittal and coronal visualization from skull to foot) 3. Complex patients are defined as and meeting any one of the subsequent criteria: 1. Radiographic criteria:
  • - PI-LL ≥ 25 degrees.
  • - TPA ≥ 30 degrees.
  • - SVA>15cm.
  • - Thoracic scoliosis ≥ 70 degrees.
  • - Thoracolumbar/lumbar scoliosis ≥ 50 degrees.
  • - Global coronal malalignment >7cm.
2. Procedural criteria:
  • - Posterior spinal fusion > 12 levels.
  • - 3 column osteotomy or ACR.
3. Geriatric criteria:
  • - Age >65 years and minimum 7 levels of spinal instrumentation during surgery.

Exclusion Criteria:

1. Age <18 years of age. 2. Active spine tumor or infection. 3. Deformity due to acute trauma. 4. Neuromuscular conditions/diseases (Parkinson's, Multiple Sclerosis, Post-polio syndrome) 5. Syndromic scoliosis. 6. Inflammatory arthritis/auto immune diseases (Rheumatoid arthritis, Lupus, Ankylosing Spondylitis) 7. Prisoners. 8. Women who are pregnant. 9. Non English speaking patients

Trial Details

Trial ID:

This trial id was obtained from ClinicalTrials.gov, a service of the U.S. National Institutes of Health, providing information on publicly and privately supported clinical studies of human participants with locations in all 50 States and in 196 countries.

NCT04194138
Phase

Phase 1: Studies that emphasize safety and how the drug is metabolized and excreted in humans.

Phase 2: Studies that gather preliminary data on effectiveness (whether the drug works in people who have a certain disease or condition) and additional safety data.

Phase 3: Studies that gather more information about safety and effectiveness by studying different populations and different dosages and by using the drug in combination with other drugs.

Phase 4: Studies occurring after FDA has approved a drug for marketing, efficacy, or optimal use.

Lead Sponsor

The sponsor is the organization or person who oversees the clinical study and is responsible for analyzing the study data.

International Spine Study Group Foundation
Principal Investigator

The person who is responsible for the scientific and technical direction of the entire clinical study.

Shay Bess, MDLawrence Lenke, MDChristopher Shaffrey, MD
Principal Investigator Affiliation Denver International Spine CenterColumbia University, Department of Orthopedic SurgeryDuke University, Departments of Neurosurgery and Orthopaedic Surgery
Agency Class

Category of organization(s) involved as sponsor (and collaborator) supporting the trial.

Other, Industry
Overall Status Recruiting
Countries Canada, United States
Conditions

The disease, disorder, syndrome, illness, or injury that is being studied.

Adult Spinal Deformity, Scoliosis, Kyphosis, Sagittal Imbalance
Additional Details

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. 1. Validation of the PROMIS tool for ASD. 2. Establish a core set of PROMs for best practice guidelines for ASD. 3. 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. 4. 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.#46; 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

Arms & Interventions

Arms

: Operative

A. Multicenter, prospective, nonrandomized analysis of operatively treated complex ASD patients meeting the following Inclusion Criteria 18 years of age or greater at the time of treatment 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: a. Radiographic criteria: i. PI-LL ≥ 25 degrees ii. TPA ≥ 30 degrees iii. SVA>15cm iv. Thoracic scoliosis ≥ 70 degrees v. Thoracolumbar/lumbar scoliosis ≥ 50 degrees vi. Global coronal malalignment >7cm b. Procedural criteria: i. Posterior spinal fusion > 12 levels ii. 3 column osteotomy or ACR c. Geriatric criteria: i. Age >65 years and minimum 7 levels of spinal instrumentation during surgery

Interventions

Procedure: - Index or spine revision surgery for complex adult spinal deformity

Surgical interventions will be patient specified by treating surgeon.

Contact a Trial Team

If you are interested in learning more about this trial, find the trial site nearest to your location and contact the site coordinator via email or phone. We also strongly recommend that you consult with your healthcare provider about the trials that may interest you and refer to our terms of service below.

La Jolla, California

Status

Recruiting

Address

Shiley Center for Orthopaedic Research and Education at Scripps Clinic

La Jolla, California, 92037

Site Contact

Tina Iannacone, MPH

[email protected]

858-554-7124

Sacramento, California

Status

Active, not recruiting

Address

University of California, Davis, Department of Orthopedic Surgery

Sacramento, California, 05616

UCSF, Department of Neurosurgery, San Francisco, California

Status

Recruiting

Address

UCSF, Department of Neurosurgery

San Francisco, California, 94143

Site Contact

Terry Nguyen

[email protected]

6184444130

Denver, Colorado

Status

Recruiting

Address

Denver International Spine Center, Rocky Mountain Hospital for Children and Presbyterian St. Luke's Medical Center

Denver, Colorado, 80218

Site Contact

Breton Line, BS

[email protected]

303-762-3472

Kansas City, Kansas

Status

Recruiting

Address

University of Kansas, Department of Orthopedic Surgery

Kansas City, Kansas, 66160

Site Contact

Stephanie Robinson

[email protected]

913-588-0581

Norton Leatherman Spine Center, Louisville, Kentucky

Status

Recruiting

Address

Norton Leatherman Spine Center

Louisville, Kentucky, 40207

Site Contact

Morgan Brown

[email protected]

6184444130

Spine Institute of Louisiana, Shreveport, Louisiana

Status

Recruiting

Address

Spine Institute of Louisiana

Shreveport, Louisiana, 71101

Site Contact

Brandi Casey

[email protected]

6184444130

Baltimore, Maryland

Status

Recruiting

Address

John Hopkins University, Department of Orthopedic Surgery

Baltimore, Maryland, 21224

Site Contact

Andrew Kim

[email protected]

6184444130

Saint Louis, Missouri

Status

Recruiting

Address

Washington University, Department of Orthopedic Surgery

Saint Louis, Missouri, 63310

Site Contact

Alison Hageman

[email protected]

6184444130

NYU, Department of Orthopedics, New York, New York

Status

Recruiting

Address

NYU, Department of Orthopedics

New York, New York, 10016

Site Contact

Connie Maglaras

[email protected]

6184444130

New York, New York

Status

Recruiting

Address

Hospital for Special Surgery, Department of Orthopedic Surgery

New York, New York, 10021

Site Contact

Desmarie Sherwood

[email protected]

6184444130

Columbia University Medical Center, New York, New York

Status

Recruiting

Address

Columbia University Medical Center

New York, New York, 10032

Site Contact

Fthimnir Hassan

[email protected]

212-932-4410

Northwell Health, New York, New York

Status

Recruiting

Address

Northwell Health

New York, New York, 10075

Site Contact

Jonathan Elysee

[email protected]

6184444130

Duke University Health System, Durham, North Carolina

Status

Recruiting

Address

Duke University Health System

Durham, North Carolina, 27710

Site Contact

Ronald Pegues

[email protected]

6184444130

University Orthopedics, Providence, Rhode Island

Status

Recruiting

Address

University Orthopedics

Providence, Rhode Island, 02905

Site Contact

Krista Szatkowski

[email protected]

6184444130

Dallas, Texas

Status

Recruiting

Address

Medical City Spine Hospital - Southwest Scoliosis Institute

Dallas, Texas, 75243

Site Contact

Brenda Olivares

[email protected]

6184444130

University of Texas - Houston, Houston, Texas

Status

Recruiting

Address

University of Texas - Houston

Houston, Texas, 77030

Site Contact

Olivia Nembhard

[email protected]

6184444130

University of Virginia, Charlottesville, Virginia

Status

Recruiting

Address

University of Virginia

Charlottesville, Virginia, 22908

Site Contact

Lorrie Sipe

[email protected]

434-924-8875

International Sites

Toronto Western, Toronto, Ontario, Canada

Status

Recruiting

Address

Toronto Western

Toronto, Ontario,

Site Contact

Sofia Magana

[email protected]

6184444130