Revision Arthroplasty

3

Review clinical trials related to Revision Arthroplasty. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Watson Extraction System for Femoral Stem Extraction

A revision total hip replacement surgery requires the surgeon to remove, or extract, the femoral stem (the rod that was placed into the thigh bone during your first hip replacement). A variety of tools and techniques can be used to do this. At The Ottawa Hospital (TOH) surgeons attempt to remove the stem using less invasive measures, such as osteotomes, a tool that separates the stem from the bone, but if it doesn't work, they may need to perform an extended trochanteric osteotomy (ETO). An ETO is more invasive and increases the risk of complications. The Watson Extraction System (WES) is another Health Canada approved tool that goes around the stem to help remove the femoral stem from the thigh bone. Research shows that the WES has been studied in case series of a few people, and the results seem promising, reducing the time of extraction and need for ETO. However, it is not clear if it offers better results than what is currently done at TOH. The purpose of this study is to compare the WES to the current/usual care care at TOH to determine whether the WES can remove the femoral stem more efficiently (in less time and at a lower hospital cost) and effectively, while improving patient safety.

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Ottawa Hospital Research InstituteUpdated: Sep 29, 2026Locations: 1
Eligibility criteria

Over 18 years of age [+2]

Tapered stem in situ less than 4 months [+3]

Status: Not yet recruiting

Persona Revision Knee System EMEA PMCF Study

The purpose of this post-market clinical follow-up study is to confirm the long-term safety, performance and clinical benefits of the Persona Revision Knee System Implants and Instrumentation in revision Total Knee Arthroplasty.

Participants needed: 238
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Zimmer, GmbHUpdated: Sep 28, 2026Locations: 2
Eligibility criteria

Patient qualifies for a revision knee arthroplasty with the Persona Revision Kne... [+6]

Patient received the study device for any condition not listed in the indication... [+19]

Status: Recruiting

Hinge vs CCK Implants

The primary purpose of this study is to compare reoperation rates for rotating hinge knee implants versus condylar constrained knee implants when used in revision total knee arthroplasty. The secondary purposes are to compare patient satisfaction, loosening rates and clinical outcomes for RHK implants compared to CCK implants in rTKA. Additionally, knee range of motion and stability will be assessed and compared at all follow-up time points. We hypothesize that RHK implants provide patients undergoing rTKA with similar reoperation rates to those of patients who receive a CCK implant. The investigators hypothesize that patients who receive an RHK implant will have similar loosening rates and clinical outcomes compared to patients who receive a CCK implant. Lastly, knee stability and patient satisfaction may improve with the use of a rotating hinge device.

Participants needed: 186
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Medstar Health Research InstituteUpdated: Sep 14, 2026Locations: 2
Eligibility criteria

Undergoing a revision total knee arthroplasty for any etiology [+8]