Robot vs. navigation: which knee surgery tech wins?
NCT ID NCT07574762
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study compares two advanced technologies used in total knee replacement: computer-assisted navigation and robotic-arm assistance. Both aim to place the new knee joint more precisely. The trial will follow 140 patients for two years to see if one method helps them forget they have an artificial knee more than the other. The goal is to find out if the extra cost and complexity of robotic surgery leads to better results.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could show that robotic-arm assistance offers no major advantage over standard navigation for knee replacement, helping surgeons choose the most effective and cost-efficient technique.
- What could go wrong
- This is a relatively small, single-center trial comparing two similar technologies. The results may not apply to all patients or surgeons, and the study is not designed to prove one method is superior.
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.
- 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 140 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2026
- Expected to finish
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Jan 2029
An estimate. End dates often move.
- 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.
- Ages
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18 years and older
- 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.
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: * Patient providing written informed consent according to regulatory requirements * Male or female patients aged ≥18 years * Patients undergoing primary total knee arthroplasty for osteoarthritis * Use of Attune® prosthesis with posterior cruciate ligament retention (CR) and patellar resurfacing Exclusion Criteria: * History of ligament reconstruction * Previous fracture or bone surgery (osteotomy) of the ipsilateral femur or tibia (except hip or ankle surgery) * Preoperative knee stiffness with flexion contracture \>15° or flexion \<90° * Individuals deprived of liberty by judicial or administrative decision * Patients not affiliated with a social security system * Patients unable to understand French * Patients with cognitive impairment * Patients whose place of residence makes close clinical follow-up impossible -- Women of childbearing potential without effective contraception * Pregnant or breastfeeding women
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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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Groupe hospitalier Diaconesses Croix Saint Simon
RECRUITINGParis, Paris, 75020, France
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