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NCT06670651Enrolling by invitation

LinkSymphoKnee (LSK) Total Knee Replacement System Study - Ultra-congruent (UC)

Source: ClinicalTrials.gov · Last updated 3 Sept 2026

Brief summary (registry, in English)

To collect information about implant performance and patient clinical outcomes in patients undergoing primary total knee arthroplasty with the LinkSymphoKnee total knee replacement system with ultra-congruent tibial bearing surface.

Status (registry)
Enrolling by invitation
Study type
Observational
Enrollment
600 (estimated)
First submitted
31 Oct 2024
Start date
21 Mar 2025
Primary completion date
Dec 2031
Lead sponsor
LinkBio Corp.
NCT number
NCT06670651

What you commit to

  • Study type: Observational
  • Planned participants: 600
  • From 21 Mar 2025 to the primary completion date, Dec 2031
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Women who are pregnant at the time of surgery,
  • Previous history of bone disease (e.g., severe osteoporosis or osteomalacia) which in the surgeon's opinion is severe enough to compromise device fixation,

Other illness

  • History of joint sepsis,
  • Systemic conditions affecting bone density (e.g., inflammatory arthritis or renal disease) which in the surgeon's opinion are severe enough to compromise device fixation,

Age

  • 80 years of age or older,

Other

  • Bone defect that requires grafting,
  • A poorly functioning contralateral total knee replacement or a contralateral revision regardless of function.

Who the study is looking for

  • 18 years or older, and skeletally mature; and
  • Undergoing a primary TKA for one or both knees using the cemented LinkSymphoKnee knee system as part of the surgeon's standard of care.
  • Able to read and understand English (because patient-reported outcome questionnaires are not validated for all potential other languages).

Age in the registry: 18 years to 79 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
OrthoAlabama Spine & Sports
Coordinator of this site? Confirm its status
BirminghamUnited StatesUnknown status
Illinois Bone and Joint Institute
Coordinator of this site? Confirm its status
LibertyvilleUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.