Osteoarthritis, rheumatoid arthritis, avascular necrosis, traumatic arthritis or other diseases requiring total knee arthroplasty or partial knee resurfacing. Musculoskeletal Diseases Arthrosis, unspecified
Conditions
Interventions
It is anticipated that the patients shall be recruited within a 12 month period at each participating centre. The length of surveillance and patient visit schedule is based on the routine procedures o
Sponsors
Stryker European Operations BV (Netherlands)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Patients requiring primary Total Knee Arthroplasty (TKA), suitable for the use of the Scorpio NRG with X3 insert or Triathlon Total Knee System with X3 insert, or, patients requiring partial knee resurfacing (unicompartmental knee) suitable for the use of the Triathlon PKR (Partial Knee Resurfacing) System with X3 insert 2. Patients who understand the conditions of the outcomes registry and are willing and able to comply with the standard post-operative evaluations and the prescribed rehabilitation 3. Patients who signed the Informed Consent Form (approved by Ethics Committee if required) prior to surgery
Exclusion criteria
Exclusion criteria: Does not meet inclusion criteria
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Survivorship of the implant; pre-operative, intra-operative and 1 year, 3 years, 5 years, 7 years and 10 years follow-up | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Any adverse event 2. Knee Society Score (KSS) 3. Knee Injury and Osteoarthritis Outcome Score (KOOS) 4. EuroQol Group Score (EQ5D) Pre-operative, intra-operative and 1 year, 3 years, 5 years, 7 years and 10 years follow-up | — |
Countries
Germany, Luxembourg, United Kingdom
Outcome results
None listed