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French Lumbar Total Disk Replacement Observational Study

NCT02381574 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 600

Last updated 2015-03-06

No results posted yet for this study

Summary

Primary Objective:

To evaluate the rate of re-operation during the first 5 years following the fitting of lumbar total disk replacement at the operated level and / or floors above and / or underlying, whatever the reasons

Conditions

  • Lumbar Total Disk Replacement

Sponsors & Collaborators

  • DePuy Synthes

    collaborator INDUSTRY

  • LDR Médical

    collaborator UNKNOWN

  • Medtronic France SAS

    lead INDUSTRY

Principal Investigators

  • Jean-Bernard SCHROEDER · SNITEM

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-06-30
Primary Completion
2020-12-31
Completion
2020-12-31

Countries

  • France

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 NCT02381574 on ClinicalTrials.gov