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Taking people in NetherlandsNo phase

Follows people with knee arthritis after an uncemented knee replacement

Studies how an uncemented ATTUNE knee implant performs in adults with knee osteoarthritis.

Plain-language title generated from the registry record
Registry title: The ATtune Knee Outcome Study

Key facts

Where
Hoofddorp, NetherlandsSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 21 and 90 years old?

Source: NCT04247672, who can take part

Where in Netherlands

  • Spaarne GasthuisHoofddorp, NetherlandsTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Spaarne Gasthuis
Trial code
NCT04247672
Record updated
27 April 2022
Original description
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.Read full original descriptionShow less

The ATtune Knee Outcome Study: Prospective Evaluation of a Novel Uncemented Rotating Platform Total Knee Arthroplasty

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.

Inclusion: 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: 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).

ClinicalTrials.gov NCT04247672