Radiographic Migration Analysis of the ATTUNE Cementless CR Fixed-Bearing Total Knee Replacement: A Multi-Center, Non-Controlled, Prospective Study
Status: Recruiting
Location: See all (3) locations...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
This is a multi-centre, single cohort trial of patients undergoing cruciate-retaining total knee arthroplasty with the Attune Cementless, Fixed Bearing, Cruciate Retaining TKA System.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 21
Healthy Volunteers: t
View:
• Symptomatic osteoarthritis of the knee indicating primary total knee arthroplasty
• Patients aged 21 years or older
• Sufficient ligamentous function to warrant retention of the posterior cruciate ligament
• Patients willing and able to comply with follow-up requirements and self-evaluations
• Ability to give informed consent
Locations
Other Locations
Canada
Nova Scotia Health - Orthopedic
NOT_YET_RECRUITING
Halifax
London Health Sciences Centre
NOT_YET_RECRUITING
London
Orthopaedic Innovation Centre
RECRUITING
Winnipeg
Contact Information
Primary
Sarah Tran
stran@orthoinno.com
204-926-1231
Backup
Shalini Hari Kumar
skumar@orthoinno.com
204-926-1232
Time Frame
Start Date: 2024-10-21
Estimated Completion Date: 2027-06
Participants
Target number of participants: 30
Treatments
Other: Attune Cementless, Fixed Bearing, Cruciate Retaining TKA System
Attune Cruciate Retaining TKA System
Related Therapeutic Areas
Sponsors
Leads: Canadian Radiostereometric Analysis Network