Robot vs. surgeon: which knee replacement heals quicker?
NCT ID NCT05744895
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at 123 people who had knee replacement surgery using the MAKO robot. Researchers tracked their pain, steps, and motion with a Fitbit and knee brace to see if robotic help leads to faster recovery compared to traditional surgery. The goal is to find out if the robot improves early outcomes like pain and movement.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- MAKO surgical robot and Triathlon knee system
- What this could lead to
- If successful, robotic-assisted knee replacement may lead to less pain and faster recovery than traditional surgery.
- What could go wrong
- This is a small, completed study comparing outcomes to a past control group, not a randomized trial. Results may not apply to all patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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123 people
The number who actually took part.
- Started
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Sep 2021
- Finished
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Jun 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
We propose to enroll patients that are scheduled for a MAKO Total knee arthroplasty
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 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 Exclusion Criteria: * 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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Washington University School of Medicine
Creve Coeur, Missouri, 63141, United States
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Other studies related to the condition(s) this trial covers.
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