About this trial

The main objectives of this study are to confirm the long-term safety, performance, and clinical benefits of the G7 Acetabular Shells when used with the Vivacit-E and Longevity HXLPE liners and instrumentation in primary and revision total hip arthroplasty.

Eligibility criteria

Qualifiers

Patient must be a legal adult who has reached full skeletal maturity.

Noninflammatory degenerative joint disease including osteoarthritis and avascular necrosis

Rheumatoid arthritis

Correction of functional deformity

Disqualifiers

Patient presents with osteoporosis, which in the opinion of the Principal Investigator, may limit the subject's ability to support total hip arthroplasty using the study device.

Patient has a metabolic disorder that may impair bone formation.

Patient has osteomalacia.

Patient has distant foci of infections which may spread to the implant site or patient with infection, sepsis or osteomyelitis.

Trial design

Treatments tested in this trial

  • Vivacit-E and Longevity (HXLPE) Liners

Treatment groups

300 Participants
are divided into 1 treatment group

Locations

11
Denmark
Copenhagen University Hospital Hvidovre2650, Hvidovre Denmark
Netherlands
Zuyderland Hospital6162 BG, Geleen Netherlands
OCON Hengelo Hengelo Netherlands
Sweden
Skane University Hospital221 85, Lund Sweden

Sponsors and collaborators

Zimmer Biomet

Lead sponsor