Robotic knee surgery vs. total knee replacement: which is better?
NCT ID NCT05290818
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compares two types of knee replacement surgery for people with advanced knee arthritis: a standard total knee replacement and a robotic-assisted partial knee replacement. The goal is to see which one leads to better knee function and is more cost-effective. About 159 adults aged 50 to 75 who are already scheduled for knee replacement will take part.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 159 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2024
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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50 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Listed for elective primary TKA for end stage medial compartment osteoarthritis * Intact anterior cruciate ligament * Full thickness and good quality lateral cartilage * Correctable intra-articular varus deformity and intact medial collateral ligament * American Society of Anesthesiologists (ASA) grades 1 and 2 * Male or female, age 50 - 75 at the time of listing for surgery * Suitable candidate for a cruciate retaining TKA (Triathlon prosthesis) and a UKA Exclusion Criteria: * Varus deformity of \> 20 degrees * Fixed flexion of \>10 degrees * Patient is unable to comply with the study protocol (incl. refusal for CT scan) or functional assessments * Female participants who are pregnant, lactating or planning pregnancy during the course of the study * Requires patella resurfacing or lateral compartment has significant OA * Inability to understand the patient information for the study, provide written informed consent or answer study questionnaires for cognitive or language reasons * Inflammatory disorder e.g. rheumatoid arthritis * Symptomatic foot, hip or spine pathology * Prior surgery (other than arthroscopy) or septic arthritis of the knee * Any other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the study,
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Nicholas Clement
RECRUITINGEdinburgh, Lothian, EH16 6SA, United Kingdom
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Digital tools may help osteoarthritis patients avoid surgery
- Could a joint injection of growth hormone and Platelet-Rich plasma offer a new path for arthritis relief?
- Can body weight predict success of knee realignment surgery?
- Can a meditation practice curb Post-Surgery pain and opioid use?
- Can a simple pill speed up knee replacement recovery?
- Can a virtual escape ease the pain of knee surgery?