Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Medacta International SA
Age
Any age
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Subjects underwent revision total knee replacement for any type of etiology (Osteoarthritis, Avascular necrosis, Rheumatoid Arthritis, Post-traumatic Arthritis, Polyarthritis, Primary implantation failure, Infection, Ligamentous Instability)
Subjects must have received a Medacta GMK Revision component using 3D metal tibial and femoral cones
Must be at minimum 1 year (12 months) post-treatment
No age limit criteria
You may not be if
Subjects with neuromuscular or neurosensory deficiency, which would limit the ability to assess the performance of the device
Subjects that were incarcerated at the time of surgery.
History of alcoholism
On chemotherapy or radiation therapy during the time of interest
Habitual use of narcotic pain medications prior to surgery or after surgery for reasons other than knee pain
History of a metabolic disorder affecting the skeletal system other than osteoarthritis or osteoporosis
History of chronic pain issues for reasons other than knee pain
Progressive local or systemic infection during time of interest
Muscular loss, neuromuscular disease, or vascular deficiency of the affected limb
Obesity or excessive weight of subject
Clareo Health | A Post-Market, Retrospective Study on 3D Metal Tibial and Femoral Cones
