Condition: Aseptic Loosening · Aseptic Loosening of Prosthetic Joint · Aseptic Loosening of Orthopaedic Hardware · Sponsor: Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
The goal of the clinical trial is to evaluate the efficacy of the AtMoves Knee System in the clinical diagnostic process of aseptic loosening in patients with a knee prosthesis. The main question it aims to answer is: Does the use of the AtMoves Knee System reduce the percentage of failed outcomes? A "failed outcome" is defined as a change in the patient-reported Knee injury and Osteoarthritis Outcome Score (KOOS-PS) that is lower than the minimal clinically important difference at 12 months. Researchers will compare two groups: The first group will undergo an additional CT scan using the AtMoves Knee System. The second group will not undergo these scans. Both groups are allowed to undergo additional diagnostic measures. Researchers will compare the percentage of "failed outcomes" between these groups. During the one-year follow-up, participants in both groups will be asked to fill out questionnaires.
This description comes directly from the study's public registry record.
Milo J.K. Mokkenstorm, MD · +31205662172 · digitalknee@amsterdamumc.nl
Always discuss trial participation with your own doctor first.
| St. Maartenskliniek | Nijmegen, Gelderland, Netherlands | Not Yet Recruiting |
| Zuyderland Ziekenhuis | Heerlen, Limburg, Netherlands | Not Yet Recruiting |
| Amphia ziekenhuis | Breda, North Brabant, Netherlands | Not Yet Recruiting |
| Amsterdam UMC | Amsterdam, North Holland, Netherlands | Recruiting |
| OCON | Hengelo, Overijsel, Netherlands | Not Yet Recruiting |
| NoordWest Ziekenhuisgroep | Alkmaar, Netherlands | Not Yet Recruiting |
| Elisabeth-TweeSteden Ziekenhuis | Tilburg, Netherlands | Not Yet Recruiting |
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Source record: clinicaltrials.gov/study/NCT06839807