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Maverick Total Disc Replacement in a 'Real World' Patient Population

NCT01338493 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 139

Last updated 2016-01-28

Study results available
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Summary

The primary purpose of the study is to document the reduction of disability after Maverick total disc replacement surgery in a 'real-world' patient population requiring disc replacement.

Conditions

  • Degenerative Disc Disease

Interventions

PROCEDURE

lumbar spinal arthroplasty + Maverick™

All patients will be subjected to a lumbar spinal arthroplasty. The anterior lumbar spine is approached through either a transperitoneal or retroperitoneal exposure. A complete anterior discectomy is performed and the Maverick™ Artificial Disc System is inserted to replace the damaged lumbar intervertebral disc.

Sponsors & Collaborators

  • Medtronic Spinal and Biologics

    lead INDUSTRY

Principal Investigators

  • Jean-Charles Le Huec, Prof. · CHU Pellegrin Tripode

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-02-28
Primary Completion
2013-07-31
Completion
2013-07-31

Countries

  • Canada
  • France
  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01338493 on ClinicalTrials.gov