Active — Not RecruitingNot Applicable

Efficacy of Robot-assisted Technique vs Conventional Technique in Preventing Early Micromobilisation After UKA

Italy50 participantsStarted 2021-10-07

Plain-language summary

The purpose of this study is to compare the percentage of early micromibilisation in unicompartmental knee arthroplasties in robot-assisted technique vs standard technique.

Who can participate

Age range

50 Years – 80 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Unicompartmental Knee Arthrosis * Femoral condyles or medial tibial plate osteonecrosis * Healthy anterior cruciate ligament, posterior cruciate ligament and collateral ligaments of the affected knee * Post traumatic loss of joint configuration * Moderate varism deformity * Patients between 50 and 80 years old * Patients able to undergo a 2-year follow up after surgery Exclusion Criteria: * Bi or Tricompartmental arthrosis * Unhealty anterior or posterior cruciate ligaments or collateral ligaments * Patients with neuromuscolar, degenerative and joint-related conditions * Patients younger than 50 * Patients older than 80 * Patients unable to undergo a 2-year follow up after surgery

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Static radiostereometric analysis (RSA)

Timeframe: Within 7 days from surgery, during hospitalisation

Static radiostereometric analysis (RSA)

Timeframe: 3 months

Static radiostereometric analysis (RSA)

Timeframe: 6 months

Static radiostereometric analysis (RSA)

Timeframe: 12 months

Static radiostereometric analysis (RSA)

Timeframe: 24 months

Trial details

NCT IDNCT05204797

SponsorIstituto Ortopedico Rizzoli

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2027-12

View on ClinicalTrials.gov More Loosening, Prosthesis trials

Who can participate

Age range

50 Years – 80 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

Static radiostereometric analysis (RSA)

Timeframe: Within 7 days from surgery, during hospitalisation

Static radiostereometric analysis (RSA)

Timeframe: 3 months

Static radiostereometric analysis (RSA)

Timeframe: 6 months

Static radiostereometric analysis (RSA)

Timeframe: 12 months

Static radiostereometric analysis (RSA)

Timeframe: 24 months