New knee implant study aims to ease arthritis pain and improve mobility
NCT ID NCT03211663
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at how well a partial knee replacement device called MOTO Medial® works for people with knee osteoarthritis. About 269 adults will be followed for several years to see if their pain, knee function, and quality of life improve after surgery. The goal is to help people with arthritis in just one part of the knee get back to daily activities with less pain.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 269 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2017
- Expected to finish
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Dec 2025
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients undergoing surgery as part of routine care.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Must be able to read, understand and provide written informed consent on the Institutional Review Board (IRB) approved Informed Consent Form (ICF). * Ability to understand and provide written authorization for use and disclosure of personal health information. * Subject who are able and willing to comply with the study protocol and follow-up visits. * Must be 18 years or older to participate. * Subjects must have medial knee disease in the affected knee compliant with the FDA-approved indications for use of MOTO Medial® UKA. * Must have had no prior arthroplasty to the medial compartment of the study knee. * Subjects must be able to return for the follow-up appointments, and have the mental capacity to cooperate and complete Patient Reported Outcome questionnaires, physical exam and radiographs. Exclusion Criteria: * Knee ligament instability (deficiency of cruciate or collateral ligaments) * Inflammatory Arthritis * History of prior knee infection * History of Alcoholism or Drug Abuse * Currently on chemotherapy or radiation therapy for neoplastic disease. Medacta MOTO Medial® Version 1 Confidential Page 9 of 36 June 5, 2017 * Currently on immunosuppressive medications including steroids * History of known sensitivity or allergy to materials used in orthopedic implants, specifically Titanium and Cobalt-Chrome alloys * Habitual use of narcotic pain medications prior to surgery (more than 3 doses or pills per week) * History of metabolic disorder affecting the skeletal system other than osteoarthritis or osteoporosis (e.g., Osteomalacia, Ricketts) * History of chronic pain issues for reasons other than knee pain. * Women who are pregnant. * Psychiatric illness * Any patient, in the opinion of the investigator, is unable to fully comply with the surgical, rehabilitation, or follow-up aspects of this procedure. * Prior joint arthroplasty on the target knee, including prior medial UKA (revision), lateral UKA, or Patellofemoral Joint * Prior high tibial osteotomy (HTO).
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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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Duke University
Durham, North Carolina, 27710, United States
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Ellis & Badenhausen Orthopaedics PSC
Louisville, Kentucky, 40223, United States
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Ortho Montana
Billings, Montana, 59102, United States
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Unova Health Clinic
Lady Lake, Florida, 32159, United States
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Whole Health Joint Replacement
Meadville, Pennsylvania, 16335, United States
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Other studies related to the condition(s) this trial covers.
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