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Completed

NCT Number: NCT02299323

INDEPENDENCE Spacer for Lumbar Fusion

The primary objective of this study is to evaluate radiographic outcomes, intra-operative parameters, clinical outcomes, and patient satisfaction following circumferential fusion using the INDEPENDENCE® integrated plate and spacer with REVOLVE® Stabilization System for the treatment of severe low back pain due to lumbar disc degeneration unresponsive to 6 months of non-operative treatment.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Scott & White Healthcare

Temple, Texas, 76508, United States

About this study

A total of thirty subjects will be enrolled at Scott & White Healthcare. The INDEPENDENCE spacer will be filled with autogenous bone graft material. The devices subject to this Agreement have received 510(k) clearance from the FDA for the indications specified in this Agreement.

Patients will be followed for 2 years with evaluations at the following time intervals: preoperatively (within 2 months of surgery) and postoperatively at 6 weeks, 3 months, 6 months, 12 months, and 24 months.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • • Objective evidence of degenerative disc disease at 1 or 2 level(s) between L2 and S1 with degeneration confirmed by patient history and radiographic examination
  • Experience pain, functional deficit and/or neurological deficit for a minimum of six months
  • Unresponsiveness to documented non-surgical treatment modalities for a minimum of six months and/or presentation with progressive symptoms of nerve root or spinal cord compression prior to enrollment
  • At least 18 years of age and maximum 65 years of age
  • Ability to provide Informed Consent for study participation and to return for all follow-up visits

Exclusion criteria

  • • Presence of systemic or localized infection at the site of surgery
  • More than 2 levels to be instrumented
  • 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 level(s) to be fused
  • More than grade 1 spondylolisthesis
  • Previous documentation of osteopenia, osteoporosis, or osteomalacia to a degree that spinal instrumentation would be contraindicated
  • 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
  • Pregnant or interested in becoming pregnant during the duration of the study
  • History of substance abuse (drugs or alcohol)
  • Any known allergy to a metal alloy
  • Mentally incompetent or prisoner
  • Currently a participant in another study

Treatment and study plan

INDEPENDENCE

Device

Lumbar Integrated plate and spacer, with percutaneous screws and rods.

Primary outcomes

  1. Radiographic fusion evaluation

    Time frame: 2 years

    Anterior Posterior / Lateral, Flexion-Extension X-rays at every timepoint will be evaluated for signs of fusion, pseudoarthrosis and implant subsidence or migration

Secondary outcomes

  1. Patient Self- Assessment for pain scores

    Time frame: 2 years

    VAS questionnaires to be completed at every follow-up timepoint

  2. Patient Satisfaction

    Time frame: 2 years

    Questionnaire to be completed at every follow-up timepoint

Sponsors and collaborators

Lead sponsor

Globus Medical Inc

Industry

Registry information

Official study title

Circumferential Lumbar Spinal Fusion for Treatment of Degenerative Disc Disease: A Prospective, Non-Randomized Clinical Study

Important dates

Study start
2012
Primary completion
2016
Study completion
2016
First posted
Nov 24, 2014
Registry last updated
Aug 10, 2016

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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