The ATtune Knee Outcome Study
To accomodate dissatisfied patients with a total knee arthroplasty (TKA) and improve outcomes, several knee systems have been developed. The cemented ATTUNE TKA shows superiority over other established knee systems at short-term, abating with longer follow-up. There have been no studies reporting on the results of the
| Condition(s) | Osteoarthritis, Knee, Knee Osteoarthritis, Knee Rheumatism, Rheumatoid Arthritis |
|---|---|
| Status | Recruiting |
| Study type | Observational |
| Summary | To accomodate dissatisfied patients with a total knee arthroplasty (TKA) and improve outcomes, several knee systems have been developed. The cemented ATTUNE TKA shows superiority over other established knee systems at short-term, abating with longer follow-up. There have been no studies reporting on the results of the uncemented version of the ATTUNE. Therefore, the main objective of the current study was to report patient reported outcome measures (PROMs), survivorship and complications associated with the uncemented ATTUNE TKA. |
| Who can participate | Inclusion Criteria: * End-stage osteoarthritis of the knee warranting joint replacement therapy. * Indicated for an ATTUNE total knee system as part of regular clinical practice. * Capability and willingness to sign informed consent and comply with follow-up procedures. * Capable enough in Dutch or English to be able to understand study procedures Exclusion Criteria: * Unable or unwilling to sign informed consent and comply with follow-up * Indication for primary revision arthroplasty * Absolute indication for cemented fixation (decreased bone stock/quality of spongiosa) |
| Ages | 21 Years to 90 Years |
| Sex | All |
| Lead sponsor | Spaarne Gasthuis |
| Locations | Hoofddorp, North Holland, Netherlands |
| Start date | 2020-02-03 |
| NCT ID | NCT04247672 |
| Official listing | https://clinicaltrials.gov/study/NCT04247672 |