Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Congenital Dislocations
  • Femur Head Necrosis
  • Hip Replacement
  • Primary and Revision Surgery
  • Primary, Secondary or Post-traumatic Osteoarthrosis
Type
Observational
Design
Observational Model: CohortTime Perspective: Prospective

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

Outcome data collected from this study will be used for Post Market Surveillance (PMS) and Clinical Evaluations on Legacy Tornier hip devices and will support peer-reviewed publications on products performance and safety at long term follow-up.

Outcome data collected from this study will be used for Post Market Surveillance (PMS) and Clinical Evaluations on Legacy Tornier hip devices and will support peer-reviewed publications on products performance and safety at long term follow-up.

Tracking Information

NCT #
NCT02230826
Collaborators
Not Provided
Investigators
Study Chair: Goulven Rochcongar, MD University Hospital, Caen