Robots vs. surgeons: which knee replacement is more precise?
NCT ID NCT03469193
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compared two ways to perform partial knee replacement for osteoarthritis: using a robotic system (Navio) versus traditional manual tools. 66 adults with knee osteoarthritis took part. The goal was to see if robotic assistance leads to better leg alignment and implant placement. Results may help improve long-term function and implant survival.
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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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66 people
The number who actually took part.
- Started
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Apr 2018
- Finished
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Jan 2022
- 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.
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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: * Male or female adult (age ≥ 18 years) * Diagnosis of unicompartmental knee osteoarthritis ( osteoarthritis internal femoral tibial (AFTI)) * Indication of unicompartmental knee arthroplasty of first intention posed Exclusion Criteria: * History of femoral or tibial osteotomy of valgization or varisation * Reconstruction of the associated cruciate ligament * Refusal to participate in the study * Pregnant women, parturient or nursing mothers * Persons deprived of their liberty by a judicial decision or administrative staff, persons under psychiatric care, persons admitted to a health or social institution to other purposes. * Major persons subject to a legal protection measure or unable to express their consent * Patient not affiliated to a social security scheme * Patient participating in another interventional research excluding routine care research (former regulation) and category 2 searches not interfering with criterion analysis main
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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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Hopital de la Croix Rousse
Lyon, 69004, France
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Other studies related to the condition(s) this trial covers.
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