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ArthroplastyNCT04786119

Study to Evaluate the Safety and Effectiveness of REAL INTELLIGENCE™ CORI™ in Knee Arthroplasty Procedures

A study testing CORI Robotics in people with Arthroplasty and Replacement, run by Smith & Nephew, Inc. at 8 sites in 4 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Background: REAL INTELLIGENCE™ CORI™ (CORI Robotics) is a computer-assisted orthopaedic surgical navigation and burring system. CORI Robotics is designed to help surgeons in planning and executing certain types of knee surgery involving bone preparation. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Arthroplasty, Replacement, Knee
What is being tested?
CORI Robotics
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
126 participants
Where
8 sitesin 4 countries
Study dates
17 Feb 2021to 10 Sep 2024
Phase
Interventional
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • The subject's treating clinician has decided that REAL INTELLIGENCE™ CORI™ and a compatible Smith+Nephew Knee Implant System is the best treatment for the subject's unicondylar knee arthroplasty (UKA) or total knee arthroplasty (TKA) and the subject has agreed to the treatment.
  • Subject requires a cemented UKA or TKA as a primary indication that meets either criterion A or B.
  • A. Subject requires a cemented UKA as a primary indication due to any of the following conditions:
  • Non-inflammatory degenerative joint disease, including osteoarthritis
  • Avascular necrosis
  • Requires correction of functional deformity
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  • Requires treatment of fractures that were unmanageable using other techniques
  • B. Subject requires a cemented TKA as a primary indication due to any of the following condition:
  • Degenerative joint disease, including osteoarthritis
  • Rheumatoid arthritis
  • Avascular necrosis
  • Requires correction of functional deformity
  • Requires treatment of fractures that were unmanageable using other techniques
  • Subject is of legal age to consent and considered skeletally mature (≥ 18 years of age at the time of surgery)
  • Subject agrees to consent to and to follow the study visit schedule (as defined in the study protocol and informed consent form), by signing the Ethical Committee (EC) or Institutional Review Board (IRB) approved informed consent form.
  • Subject plans to be available through one (1) year postoperative follow-up.
  • Routine radiographic assessment is possible.
  • Subject able to follow instructions and deemed capable of completing all study questionnaires.

Who cannot join

  • Subject receives a CORI Robotics UKA or TKA on the index joint as a revision for a previously failed surgery, or need for complex implants, or any other implant than a standard UKA or TKA (e.g. stems, augments, or custom made devices).
  • Subject has been diagnosed with post-traumatic arthritis
  • Subject receives bilateral UKA or TKA
  • Subject does not understand the language used in the Informed Consent Form.
  • Subject does not meet the indication or is contraindicated for UKA or TKA according to specific Smith+Nephew knee system's Instructions For Use (IFU).
  • Subject has active infection or sepsis (treated or untreated).
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  • Subject is morbidly obese with a body mass index (BMI) greater than 40.
  • Subject is pregnant or breast feeding at the time of surgery.
  • Subject, in the opinion of the Investigator, has advanced osteoarthritis or joint disease at the time of surgery and was better suited for an alternate procedure.
  • Subject has a condition(s) that may interfere with the TKA or UKA survival or outcome (i.e., Paget's or Charcot's disease, vascular insufficiency, muscular atrophy, uncontrolled diabetes, moderate to severe renal insufficiency or neuromuscular disease, or an active, local infection).
  • Subject in the opinion of the Investigator, has an emotional or neurological condition that would pre-empt their ability or willingness to participate in the study including mental illness, mental retardation, drug or alcohol abuse.
  • Subject, in the opinion of the Investigator, has a neuromuscular disorder that prohibited control of the index joint.
  • Subject is a prisoner or meets the definition of a Vulnerable Subject per ISO 14155 Section 3.55.

Trial locations and contacts

8 sites in 4 countries.

8 sites in 4 countries

United States4 sites
  • Duke Health

    Morrisville, North Carolina, 27560

  • OrthoNeuro

    New Albany, Ohio, 43054

  • Orthopedic Institute of the West

    Phoenix, Arizona, 85054

  • Oregon Health & Science University

    Portland, Oregon, 97239

Other trials in United States

Germany2 sites
  • Orthopaedic clinic of the Medical School Hannover

    Hanover, 30625

  • Pius-Hospital Oldenburg

    Oldenburg, 26121

Other trials in Germany

India1 site
  • Lokmanya Hospital

    Pune, Maharashtra, 411044

Other trials in India

United Kingdom1 site
  • The Royal Orthopaedic Hospital NHS Foundation Trust

    Birmingham, West Midlands, B31 2AP

Other trials in United Kingdom

About this study

Official title: A Prospective, Multi-center, Study to Evaluate the Safety and Effectiveness of REAL INTELLIGENCE™ CORI™ in Unicondylar Knee Arthroplasty (UKA) and Total Knee Arthroplasty (TKA) Procedures

Background: REAL INTELLIGENCE™ CORI™ (CORI Robotics) is a computer-assisted orthopaedic surgical navigation and burring system. CORI Robotics is designed to help surgeons in planning and executing certain types of knee surgery involving bone preparation. These types of surgery are called 'unicondylar knee arthroplasty' (UKA) and 'total knee arthroplasty' (TKA).

Purpose:

Read more

This study is being carried out to demonstrate the safety and effectiveness of the CORI Robotics. The data collected will be used to meet the post-market clinical follow-up requirement in Europe and to support claims and publications.

Objectives:

The primary objective of this study is to evaluate the use of CORI Robotics in UKA and TKA procedures in achieving post-operative leg alignment to check that the results of the operation are similar to what the surgeon originally planned.

Research participants / locations:

Research participants will be recruited from up to 8 sites in 4 countries globally (UK, US, Germany and India).

Being tested
CORI Robotics
Keywords
Unicompartmental Knee Arthroplasty, Total Knee Arthroplasty

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • CORI RoboticsDevice

    Knee arthroplasty with robotics assisted surgery using the CORI Robotics System.

Study groups in NCT04786119
Study groupRoleWhat they receive
CORI RoboticsExperimentalSubjects having robotic assisted knee arthroplasty as decided by their doctor and treated with CORI Robotics.
Receives: Device: CORI Robotics

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Post-Operative Leg Alignment

    The number of participants with knees achieving post-operative leg alignment was taken by radiographic assessment at 6 weeks. Post-operative leg alignment was achieved when the deviation from the participant specific target did not exceed ±3 degrees. Participants achieving post-operative leg alignment were categorized by the following procedure types: Unicondylar Knee Arthroplasty (UKA), Total Knee Arthroplasty (TKA), and overall (i.e., both procedures).

    Measured: 6 weeks

  2. Percentage of Knees Achieving Post-Operative Leg Alignment

    The percentage of knees achieving post-operative leg alignment taken by radiographic assessment at 6 weeks. Post-operative leg alignment was achieved when the deviation from the participant specific target did not exceed ±3 degrees. Percentage of knees achieving post-operative leg alignment were categorized by the following procedure types: Unicondylar Knee Arthroplasty (UKA), Total Knee Arthroplasty (TKA), and overall (i.e., both procedures).

    Measured: 6 weeks

Secondary outcomes (13)
  1. Component Alignment: Femoral Antero-Posterior (A/P) Angle

    Component alignment assessed on long leg standing antero-posterior (A/P) X-rays and standard non weight bearing lateral X-rays taken 6 weeks after surgery. From the A/P radiograph, the femoral flexion angle is to be obtained using standard radiographic tools. Femoral flexion angle is defined as the angle formed between a line across the base of the femoral condyles and a line that is centered along the femoral canal.

    Measured: 6 weeks

  2. Component Alignment: Tibial Antero-Posterior (A/P) Angle

    Component alignment assessed on long leg standing antero-posterior (A/P) X-rays and standard non weight bearing lateral X-rays taken 6 weeks after surgery. From the A/P radiograph, the tibial angle denotes the angle formed on the medial side of the knee from intersecting lines parallel to the tibial base plate and a line drawn parallel to the tibial canal.

    Measured: 6 weeks

  3. Component Alignment: Total Valgus Angle

    Component alignment assessed on long leg standing antero-posterior (A/P) X-rays and standard non weight bearing lateral X-rays taken 6 weeks after surgery. The total valgus angle is the sum of the femoral flexion angle and the tibial angle.

    Measured: 6 weeks

  4. Component Alignment: Femoral Flexion Angle

    Component alignment assessed on long leg standing antero-posterior (A/P) X-rays and standard non weight bearing lateral X-rays taken 6 weeks after surgery. The lateral view femoral flexion angle is obtained from the intersection of a line from the center of the femoral implant to the top of the femur with a line through the femoral canal. The angle is measured on the proximal side of the intersection.

    Measured: 6 weeks

  5. Component Alignment: Tibial Lateral Angle

    Component alignment assessed on long leg standing antero-posterior (A/P) X-rays and standard non weight bearing lateral X-rays taken 6 weeks after surgery. The lateral view tibial angle is the angle obtained from the intersection of a line drawn parallel to the bottom of the tibial base insert and a line through the center of the tibial base and the tibial canal.

    Measured: 6 weeks

  6. Radiographic Assessment: Radiographic Findings

    Radiographic assessment on antero-posterior (A/P) and lateral (L) views were performed to identify radiographic findings for the presence of radiolucent lines, osteolysis and implant migration. The number of participants with radiographic findings were categorized as one of the following:

    • Yes
    • No
    • Missing

    Measured: 12 months

  7. 2011 Knee Society Score (KSS): Objective Score

    The 2011 Knee Society Score Objective score is completed by the surgeon and assesses the condition of the knee based on factors like pain, alignment, ligament stability, and range of motion. The Objective score ranges from 0 to 100, with a higher score indicating better knee function (i.e., a better outcome).

    Measured: Pre-op, 6 weeks, 6 months and 12 months

  8. 2011 Knee Society Score (KSS): Function Score

    The 2011 Knee Society Score Function assesses the participant's ability to perform daily activities and is a component of the overall KSS evaluation. The Function score ranges from 0 to 100, with a higher score indicating better function (i.e., a better outcome).

    Measured: Pre-op, 6 weeks, 6 months and 12 months

  9. 2011 Knee Society Score (KSS): Satisfaction Score

    The 2011 Knee Society Score Satisfaction score is a five question 40-point scale completed by the participant. The Satisfaction score ranges from 0 to 40, with a higher score indicating greater satisfaction (i.e., a better outcome).

    Measured: Pre-op, 6 weeks, 6 months and 12 months

  10. Oxford Knee Score (OKS)

    The Oxford Knee Score (OKS) specifically assesses the patient's perspective following knee arthroplasty surgery to indicate knee function. Total overall scores range from 0 to 48. A score of 0 is the worst possible outcome while a score of 48 indicates the best possible outcome.

    Measured: Pre-op, 6 weeks, 6 months and 12 months

  11. Forgotten Joint Score (FJS)

    The forgotten Joint Score (FJS) consisted of 12 questions with responses recorded using a five-point Likert response format: "Never", "almost never", "seldom", "sometimes" and "mostly". The item scores were summed and linearly transformed to a 0 to 100 scale and then reversed with a high value reflecting the ability of the subject to forget about the replaced knee joint during the activities of daily living. A score of 100 is the best possible outcome (i.e., a high score indicated a better outcome).

    Measured: 6 weeks, 6 months and 12 months

  12. Five-level EuroQol Five-dimensional (EQ-5D-5L) Visual Analogue Scale (VAS) Score

    The EQ-5D-5L is composed of the EQ-5D-5L descriptive system and the EQ Visual Analogue scale (EQ VAS). The EQ VAS score uses a scale from 0 to 100, with 0 indicating 'the worst health you can imagine' (i.e., a worse outcome) and 100 indicating 'the best health you can imagine' (i.e., a better outcome).

    Measured: Pre-op, 6 weeks, 6 months and 12 months

  13. Five-level EuroQol Five-dimensional (EQ-5D-5L) Index Score

    The EQ-5D-5L is composed of the EQ-5D-5L descriptive system (i.e., index score) and the EQ Visual Analogue scale (EQ VAS). The descriptive system is a health-related quality of life score that comprises 5 dimensions (mobility, self care, usual activities, pain/discomfort, anxiety/depression). Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems, and extreme problems. Responses are coded as single-digit numbers expressing the severity level selected in each dimension. A score of 1 indicates perfect health-related quality of life and 0 indicates no health-related quality of life (i.e., a higher score is a better outcome). Index scores cannot be greater than 1 but could be less than 0.

    Measured: Pre-op, 6 weeks, 6 months and 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Mar 2021
  2. Study start17 Feb 2021
  3. Primary completion27 Oct 2023
  4. Study completion10 Sep 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
126 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04786119
Sponsor's protocol ID
CORI.2019.07
Status last verified
Sep 2024
First submitted
3 Mar 2021
Last updated
31 Oct 2025
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing CORI Robotics in people with Arthroplasty and Replacement, run by Smith & Nephew, Inc. at 8 sites in 4 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 18 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 31 Oct 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 8 sites in United States, Germany, India, United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Yes. Results are posted in the registry (first posted 13 Jan 2025). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Post-Operative Leg Alignment (time frame: 6 weeks). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 31 Oct 2025.

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