MAKO Total Knee Artroplasty
Completed
Conditions studied: Osteoarthritis, Knee
In brief
The purpose of this study is to determine the early clinical and radiographic outcomes of robotically assisted total knee arthroplasty with the MAKO surgical robot using the Triathlon knee system. Results of this study will be compared to those of a previously published cohort of patients from this institution who underwent TKA using non-robotic, manual instruments. MAKO TKA patients will be given Fitbits and the Focus Motion Knee Brace to capture the data listed in attachment section. The results of this data will be compared to the control group to see if there is or there is not a difference in clinical outcomes with patients receiving Total knee surgery using the MAKO surgical robot versus those who got Total knee surgery without the MAKO robot.
Key facts
- Study ID
- NCT05744895
- Run by
- Washington University School of Medicine
- People needed
- 123
- Starts
- 2021-09-14
- Expected to finish
- 2025-06-30
- Last updated by the study team
- 2026-02-17
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Planning to undergo Unilateral primary total knee arthroplasty
- 18 and up
- Willing to sign informed consent
- Willing to return for all follow-up visits
- Smartphone or tablet device capable of running the Fitbit andFocusMotion platform
You may not qualify if…
- BMI > 45
- Inflammatory arthritis
- Narcotic use greater than 5 days per week
- Walking aid for musculoskeletal or neurologic issue other than operative joint
- Bilateral total knee arthroplasty
- Patient with an active infection or suspected infection in the operative joint
- The absolute and relative contraindications stated in the FDA cleared labeling for the device
Where it is running
- Washington University School of Medicine — Creve Coeur, Missouri, United States
Full record on ClinicalTrials.gov
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