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Proximal Junctional Kyphosis Following Long Instrumented Spinal Fusion: The Effect of Implant Selection (PJK)

Primary Purpose

Kyphosis

Status
Withdrawn
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Less rigid rod
Rigid Rod
Sponsored by
Globus Medical Inc
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Kyphosis focused on measuring Rigid rods, less rigid rods, prevent kyphosis, long constructs

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Adult patients with degenerative spondylolisthesis with objective evidence of neurologic impairment, kyphosis, and failed previous fusion (pseudoarthrosis) requiring treatment with an instrumented posterior fusion from the thoracolumbar junction (T10-L1) to the sacrum
  • At least 18 years of age and maximum 70 years of age
  • Ability to provide Informed Consent for study participation and patients to return for all follow-up visits

Exclusion Criteria:

  • Presence of systemic or localized infection
  • Previous fusion attempt at the involved level(s)
  • More than three previous open, posterior, lumbar spinal surgical procedures at the involved level(s)
  • Trauma at the levels to be fused
  • Previous documentation of osteopenia or osteomalacia
  • Diagnosis of a condition or requires postoperative medication(s), which may interfere with bony/soft tissue healing
  • Presence of a disease entity or condition which totally precludes possibility of bony fusion (e.g. metastatic cancer, HIV, long term use of steroids, etc.)
  • Immunosuppressive disorder
  • Pregnancy
  • History of alcohol and/or drug abuse
  • Any known allergy to a metal alloy
  • Mentally incompetent or prisoner
  • Currently a participant in another study
  • Preoperative structural deformity in the thoracic spine (kyphosis >60 degrees, Coronal curve >40 degrees)
  • Circumferential fusion above L1

Sites / Locations

  • Peachtree Neurosurgery
  • Department of Neurosurgery, University of Michigan
  • Department of Orthopedic Surgery, University of Copenhagen, Denmark

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Less rigid rods

Rigid Rods

Arm Description

Titanium rods that have a soft, plastic end

Titanium rods

Outcomes

Primary Outcome Measures

Evidence of Proximal Junction Kyphosis as determined by radiographic measurements during follow up visits
Radiographs will be taken to measure lumbar lordosis, adjacent segment kyphosis, thoracolumbar kyphosis, sagittal balance, Sacral slope and pelvic incidence.

Secondary Outcome Measures

Patient outcome measures
Forms to be completed at follow up visits will include VAS, SRS 22, SF12, ODI, Patient Satisfaction, Work Status Assessment and Odom's criteria.

Full Information

First Posted
September 26, 2011
Last Updated
July 31, 2019
Sponsor
Globus Medical Inc
Collaborators
University of Michigan, Polaris Spine and Neurosurgery Center
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1. Study Identification

Unique Protocol Identification Number
NCT01441999
Brief Title
Proximal Junctional Kyphosis Following Long Instrumented Spinal Fusion: The Effect of Implant Selection
Acronym
PJK
Official Title
Proximal Junctional Kyphosis Following Long Instrumented Spinal Fusion: The Effect of Implant Selection
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Withdrawn
Why Stopped
principal investigator decision
Study Start Date
October 2011 (undefined)
Primary Completion Date
December 2016 (Actual)
Study Completion Date
March 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Globus Medical Inc
Collaborators
University of Michigan, Polaris Spine and Neurosurgery Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The treatment of adult deformity has improved with the development and use of modern segmental instrumentation, including posterior instrumentation. However, the incidence of proximal junctional kyphosis (PJK) caused by the accelerated degeneration of the joint capsules and smaller articular processes in the proximal junctional region has also been noted. One potential way of decreasing PJK is to decrease the structural rigidity of the construct at the top thereby providing a transition to the non-instrumented spine and allowing for less facet capsule and muscle disruption.
Detailed Description
While a possible solution to PJK is to reduce structural rigidity at the top of the construct, there is a need to investigate it. In the proposed study, the investigators will compare the rate of proximal junctional kyphosis in patients treated with a stainless steel rod (REVERE Stabilization System) versus those treated with TRANSITION Stabilization System. Patient outcome measures (Scoliosis Research Society (SRS-22), SF12 and ODI) and radiographic measurements (including lumbar lordosis (L1-S1), adjacent segment kyphosis, thoracolumbar kyphosis (T10-L2), sagittal balance, sacral slope, and pelvic incidence) will be analyzed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Kyphosis
Keywords
Rigid rods, less rigid rods, prevent kyphosis, long constructs

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Less rigid rods
Arm Type
Active Comparator
Arm Description
Titanium rods that have a soft, plastic end
Arm Title
Rigid Rods
Arm Type
Active Comparator
Arm Description
Titanium rods
Intervention Type
Device
Intervention Name(s)
Less rigid rod
Other Intervention Name(s)
TRANSITION
Intervention Description
Titanium rod with semi rigid end
Intervention Type
Device
Intervention Name(s)
Rigid Rod
Other Intervention Name(s)
REVERE
Intervention Description
Rigid Titanium rods
Primary Outcome Measure Information:
Title
Evidence of Proximal Junction Kyphosis as determined by radiographic measurements during follow up visits
Description
Radiographs will be taken to measure lumbar lordosis, adjacent segment kyphosis, thoracolumbar kyphosis, sagittal balance, Sacral slope and pelvic incidence.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Patient outcome measures
Description
Forms to be completed at follow up visits will include VAS, SRS 22, SF12, ODI, Patient Satisfaction, Work Status Assessment and Odom's criteria.
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Adult patients with degenerative spondylolisthesis with objective evidence of neurologic impairment, kyphosis, and failed previous fusion (pseudoarthrosis) requiring treatment with an instrumented posterior fusion from the thoracolumbar junction (T10-L1) to the sacrum At least 18 years of age and maximum 70 years of age Ability to provide Informed Consent for study participation and patients to return for all follow-up visits Exclusion Criteria: Presence of systemic or localized infection Previous fusion attempt at the involved level(s) More than three previous open, posterior, lumbar spinal surgical procedures at the involved level(s) Trauma at the levels to be fused Previous documentation of osteopenia or osteomalacia Diagnosis of a condition or requires postoperative medication(s), which may interfere with bony/soft tissue healing Presence of a disease entity or condition which totally precludes possibility of bony fusion (e.g. metastatic cancer, HIV, long term use of steroids, etc.) Immunosuppressive disorder Pregnancy History of alcohol and/or drug abuse Any known allergy to a metal alloy Mentally incompetent or prisoner Currently a participant in another study Preoperative structural deformity in the thoracic spine (kyphosis >60 degrees, Coronal curve >40 degrees) Circumferential fusion above L1
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bryan Cunningham, PhD
Organizational Affiliation
Globus Medical Inc
Official's Role
Study Director
Facility Information:
Facility Name
Peachtree Neurosurgery
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30342
Country
United States
Facility Name
Department of Neurosurgery, University of Michigan
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109-0338
Country
United States
Facility Name
Department of Orthopedic Surgery, University of Copenhagen, Denmark
City
Copenhagen
ZIP/Postal Code
2100
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
16025035
Citation
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Results Reference
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PubMed Identifier
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Citation
Hee HT, Yu ZR, Wong HK. Comparison of segmental pedicle screw instrumentation versus anterior instrumentation in adolescent idiopathic thoracolumbar and lumbar scoliosis. Spine (Phila Pa 1976). 2007 Jun 15;32(14):1533-42. doi: 10.1097/BRS.0b013e318067dc3d.
Results Reference
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PubMed Identifier
18580741
Citation
Hollenbeck SM, Glattes RC, Asher MA, Lai SM, Burton DC. The prevalence of increased proximal junctional flexion following posterior instrumentation and arthrodesis for adolescent idiopathic scoliosis. Spine (Phila Pa 1976). 2008 Jul 1;33(15):1675-81. doi: 10.1097/BRS.0b013e31817b5bea.
Results Reference
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PubMed Identifier
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Citation
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Results Reference
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PubMed Identifier
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Citation
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Citation
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Citation
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Citation
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Citation
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Proximal Junctional Kyphosis Following Long Instrumented Spinal Fusion: The Effect of Implant Selection

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