Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Stryker Orthopaedics
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Patient has signed an Institutional Review Board (IRB) approved, study specific Informed Patient Consent Form.
Patient is a male or non-pregnant female age 18 years or older at time of study device implantation.
Patient is a candidate for revision of all femoral and tibial components of a total knee replacement.
Patient is willing and able to comply with postoperative scheduled clinical and radiographic evaluations and rehabilitation.
You may not be if
Patient has a Body Mass Index (BMI) \> 40.
Patient has an active or suspected latent infection in or about the affected knee joint at time of study device implantation.
Patient has a neuromuscular or neurosensory deficiency, which limits the ability to evaluate the safety and efficacy of the device.
Patient is diagnosed with a systemic disease (e.g. Lupus Erythematosus) or a metabolic disorder (e.g. Paget's Disease) leading to progressive bone deterioration.
Patient is immunologically suppressed or receiving steroids in excess of normal physiological requirements (e.g. \> 30 days).
Patient has a failed unicondylar knee prosthesis.
Patient has a known sensitivity to device materials.
Patient is a prisoner.
Clareo Health | Triathlon Total Stabilizer (TS) Outcomes Study
