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PRESTIGE Observational Study

NCT00875810 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 194

Last updated 2016-01-28

Study results available
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Summary

Prestige artificial disc replacement is an alternative treatment option with 16 years of experience addressing the unmet needs of surgical fusion interventions. Previous studies on the PRESTIGE® cervical disc have proven the safety and effectiveness of artificial disc surgery with level I evidence.

The PRESTIGE Observational Study is intended to collect prospectively observational data primarily on the Quality of Life (QoL).

Conditions

  • Degenerative Cervical Disc Disease

Sponsors & Collaborators

  • Medtronic Spinal and Biologics

    lead INDUSTRY

Principal Investigators

  • Jan Štulik, MUDr · University Clinic Motol

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-04-30
Primary Completion
2013-11-30
Completion
2013-11-30

Countries

  • Czechia
  • Greece
  • Hungary
  • Kuwait
  • Poland
  • Saudi Arabia
  • Serbia
  • Slovakia

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 NCT00875810 on ClinicalTrials.gov