Comparative Effectiveness of the Journey Total Knee Arthroplasty Relative to Two Standard of Care Total Knee Arthroplasty Prostheses: A Randomized Controlled Trial
Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
The purpose of the study is to determine if knee replacement performed using Journey II implant is different from two other standard-of-care knee replacements using Stryker and Zimmer in terms of knee movements and forces, walking patterns, pain, and function after surgery.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Maximum Age: 75
Healthy Volunteers: f
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• Participant has signed an approved informed consent form.
• Participant is a male or non-pregnant female and aged 50 to 75 years at the time of study device implantation.
• Participant has a diagnosis of Non-Inflammatory Degenerative Joint Disease (NIDJD).
• Participant is a candidate for a primary posterior-stabilized total knee replacement.
• Participant is willing and able to comply with postoperative scheduled clinical and radiographic evaluations and rehabilitation.
Locations
Other Locations
Canada
Edmonton Bone and Joint Centre
RECRUITING
Edmonton
Contact Information
Primary
Ailar Ramadi, PhD
Ailar.Ramadi@albertahealthservices.ca
780-492-6713
Time Frame
Start Date: 2019-09-09
Estimated Completion Date: 2027-12
Participants
Target number of participants: 75
Treatments
Experimental: Journey II
Smith and Nephew Richards (SNR) Journey II Knee prosthesis
Active_comparator: Stryker
Stryker Triathlon Total Knee prosthesis
Active_comparator: Zimmer
Zimmer Persona® The Personalized Knee prosthesis
Related Therapeutic Areas
Sponsors
Leads: University of Alberta