Status:
COMPLETED
Comparison of Alignment Achieved Using the VELYS Robotic-Assisted Solution Versus Manual Instrumentation in Total Knee Arthroplasty
Lead Sponsor:
DePuy Orthopaedics
Conditions:
Osteo Arthritis Knee
Osteoarthritis
Eligibility:
All Genders
22-85 years
Phase:
NA
Brief Summary
The purpose of this post-market research study is to gather clinical and radiographic (X-ray) information about total knee replacement surgeries completed with the VELYS Robotic-Assisted Solution and ...
Eligibility Criteria
Inclusion
- Subject is male or female and between the ages of 22 and 85 years at the time of consent, inclusive.
- Subject has a severely painful and/or severely disabled joint resulting from osteoarthritis, post-traumatic arthritis or rheumatoid arthritis and in the opinion of the Investigator, is a suitable candidate for primary TKA using the devices described in this CIP with either resurfaced or non-resurfaced patellae.
- Subject that is willing to give voluntary, written informed consent to participate in this clinical investigation and authorize the transfer of his/her information to the Sponsor
- Subject is currently not permanently bedridden, as determined by the Investigator
- Subject, in the opinion of the Investigator, is able to understand this clinical investigation and is willing and able to perform all study procedures and follow-up visits and co-operate with investigational procedures.
- Subject is able to read and comprehend the Informed Consent Document as well as complete the required PROs in English.
- Subject's pre-operative alignment is such that (in the opinion of the Investigator) it is appropriate for it to be adjusted to mechanical long leg alignment during surgery.
Exclusion
- The Subject is a woman who is pregnant or lactating.
- Contralateral knee has already been enrolled in this study.
- Subject had a contralateral amputation.
- Previous partial knee replacement (unicompartmental, bicompartamental or patellofemoral joint replacement), patellectomy, high tibial osteotomy or primary TKA in affected knee.
- Subject has an active local or systemic infection
- Subject has loss of bone or musculature, osteoporosis, neuromuscular compromise or vascular deficiency in the affected limb in sufficient degree to render the procedure unjustifiable in the opinion of the Investigator (e.g. absence of musculo-ligamentous supporting structures, joint neuropathy)
- Subject has severe instability secondary to advanced loss of osteochondral structure or the absence of collateral ligament integrity.
- Subject has participated in a clinical investigation with an investigational product (drug or device) in the last three (3) months.
- Subject is currently involved in any personal injury litigation, medical-legal or worker's compensation claims.
Key Trial Info
Start Date :
February 23 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 6 2023
Estimated Enrollment :
200 Patients enrolled
Trial Details
Trial ID
NCT04730271
Start Date
February 23 2021
End Date
September 6 2023
Last Update
April 27 2025
Active Locations (5)
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1
Sinai Hospital of Baltimore
Baltimore, Maryland, United States, 21215
2
Cuyuna Regional Medical Center
Crosby, Minnesota, United States, 56441
3
OrthoCarolina
Charlotte, North Carolina, United States, 28207
4
Campbell Clinic
Germantown, Tennessee, United States, 38138