The ATtune Knee Outcome Study
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age21-90
SponsorSpaarne Gasthuis
About this trial
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.
Eligibility criteria
Qualifiers
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
Disqualifiers
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)
Trial design
Treatments tested in this trial
- Total Knee Arthroplasty (uncemented rotating platform ATTUNE)
Treatment groups
No treatment groups listed
Sponsors and collaborators
Source ClinicalTrials.gov