Safety and Performance Study of the CAdiscTM-L Lumbar Spinal Disc Replacement Device For CE Marking (DISCERN)

Debilitating Low Back paIn: Multi-centre Safety and performanCe invEstigation Of CAdiscTM-L, Total Disc ReplacemeNt Therapy

The purpose of this European Union (EU) study to evaluate the safety and performance of the CAdiscTM-L Lumbar Spinal Disc Replacement Device in the surgical replacement of the lumbar intervertebral discs (L3 to S1) for patients requiring surgical intervention for total lumbar disc replacement for the treatment of debilitating, chronic low back pain.

Study Overview

• Status: Completed
• Conditions: Chronic Low Back Pain; Lumbar Degenerative Disc Disease
• Intervention / Treatment: Device: CAdisc™-L (Total Disc Replacement)

Detailed Description

Study Design: International, multicenter, open, clinical investigation with comparison to pre-operative

Currently there are two surgical procedures for the treatment of chronic low back pain: Spinal fusion and Total Disc Replacement. CAdisc™-L(Compliant Artificial disc - Lumbar) is a Lumbar total disc replacement product that preserves motion and restores disc height and stability

Surgical access is via a routine anterior approach with discectomy (removal of the diseased disc), which is performed prior to implantation of the CAdisc™-L. Instruments are then used to prepare the disc space and to controllably place the replacement disc at the target point. It is not intended for the surgery to differ in type, duration or risk to any other device of this nature.

• Study Type: Interventional
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Belgium
  • Antwerp, Belgium
• Germany
  • Bogen, Germany
• Netherlands
  • Zwolle, Netherlands
• United Kingdom
  • Aberdeen, United Kingdom

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 25 years to 65 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Male or non pregnant, non-lactating female
• Aged between 25-65 years (inclusive)
• BMI < 35
• Preoperative ODI > 30 points
• Chronic low back pain, and is in the opinion of the investigator a suitable candidate for anterior lumbar surgery
• Completed at least 6 months of conservative treatment without obtaining adequate symptomatic relief

• Degenerative disc changes at a single level between L3 - L4, or L4 - L5, or L5 - S1 as confirmed by positive discography and visualized by X-Ray, CT or MRI scan and/or with one or more of the following:

  • Decrease in disc height < 50% (or up to 80% and no benefit from facet injections)
  • Annular thickening
  • Herniated nucleus pulpous
• Subject is able to give voluntary, written informed consent to participate in this investigation and from whom written consent must be obtained prior to enrolment.

Exclusion Criteria:

• Back or leg pain of unknown aetiology
• Radicular or sciatic pain which is more severe than low back pain
• Previous lumbar spinal surgery which could affect the trial outcome (e.g., disc replacement)
• Obvious signs of psychological or worker's compensation or litigation claim elements to their condition, or are actively engaged in such activities
• Subject is unwilling or unable to give consent or adhere to the follow-up programme
• Active infection or metastatic disease
• Non-degenerative spondylolisthesis
• Degenerative spondylolisthesis > grade 1
• Known allergy to any of the implant materials
• Osteoporosis (if suspected to be confirmed by bone density being 2.5SD below normal as assessed using DEXA analysis in post-menopausal females if suggested by X-ray or other risk factors)
• Osteopenia
• Bony lumbar stenosis
• Pars defect
• Isolated radicular compression syndromes, especially due to disc herniation
• Clinically compromised vertebral bodies at the affected levels due to current or past trauma
• Subject is skeletally immature as determined by the investigator
• Subject has participated in another clinical investigation or study with an investigational medical device within the last 60 days
• Concomitant medications that are known significantly to interfere with bone/soft tissue healing, e.g. steroids.
• Uncorrected iliac, aorto-iliac, or aortic aneurysm disease.
• Spinal instability (> 3mm translation or > 5° angulation) confirmed by functional radiological assessment.
• Degenerative disc changes at the L6 - S1 level

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Improvement of 15 points on the Oswestry Disability Index (ODI) scale at 3 months post-surgery, compared to baseline

Collaborators and Investigators

• Sponsor: Ranier Technology Limited

Study record dates

Study Major Dates

• Study Start: October 1, 2009
• Study Completion (Actual): June 1, 2010

Study Registration Dates

• First Submitted: July 30, 2009
• First Submitted That Met QC Criteria: July 30, 2009
• First Posted (Estimate): July 31, 2009

Study Record Updates

• Last Update Posted (Estimate): October 15, 2010
• Last Update Submitted That Met QC Criteria: October 14, 2010
• Last Verified: October 1, 2010

More Information

Terms related to this study

• Keywords: Spine surgery
• Additional Relevant MeSH Terms: Pain; Neurologic Manifestations; Musculoskeletal Diseases; Spinal Diseases; Bone Diseases; Back Pain; Low Back Pain; Intervertebral Disc Degeneration
• Other Study ID Numbers: Ranier01/2008