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Arthroplasty clinical trials

View clinical trials related to Arthroplasty.

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NCT ID: NCT05824533 Terminated - Arthroplasty Clinical Trials

Difference in Patellar Tracking Before and After Journey II BCS Total Knee Arthroplasty, Evaluated With 4D CT Imaging

Start date: April 8, 2022
Phase: N/A
Study type: Interventional

The current proposal aims to investigate the patellar tracking in adult patients receiving Journey II Bi-Cruciate Stabilized (BCS) total knee arthroplasty (TKA) before and one year after surgery, positioned with the CORI Robotics System instrumentation. The hypothesis is that less change in patella tracking before and after surgery will lead to less anterior knee pain complaints. Patella tracking is investigated using 4Dimensional Computer Tomography (4D CT) imaging. Researchers will compare the group of participants that will receive a patella onlay button with the group that will not receive a patella onlay button with their TKA to see if there is a difference in motion and pain experienced by the participants.

NCT ID: NCT04618770 Terminated - Arthroplasty Clinical Trials

Triathlon PSR Outcomes Study

Start date: February 8, 2021
Phase: N/A
Study type: Interventional

This study is a prospective, open-label, post-market, non-randomized, multi-center clinical evaluation of the Triathlon Total Knee System using the Triathlon PSR Tibial Insert for primary total knee arthroplasty (TKA) in a consecutive series of patients who meet the eligibility criteria. The SF-36 score of subjects receiving the Triathlon Total Knee with the Triathlon PSR insert is expected to be comparable with that of subjects receiving historical Triathlon PS cemented constructs.

NCT ID: NCT04089371 Terminated - Shoulder Pain Clinical Trials

A Post-Market Clinical Evaluation of the ReUnion Reversible Fracture (RFX) System

Start date: October 1, 2019
Phase:
Study type: Observational

This investigation is a prospective, multi-center clinical investigation. It is anticipated that a total of one hundred (100) subjects will be enrolled at approximately 5-10 sites. The clinical investigation has been designed to follow the surgeon's standard of care for joint arthroplasty patients, which entails clinical evaluation on a regular ongoing basis, or as needed should the patient become symptomatic in the treated joint.

NCT ID: NCT02713906 Terminated - Arthroplasty Clinical Trials

Materialise X-ray Knee Guides for Total Knee Arthroplasty

Start date: September 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the positioning of customized guides designed from patients X-Rays (Materialise X-Ray Knee Guides) using computed tomography in primary total knee arthroplasty.

NCT ID: NCT01740999 Terminated - Arthroplasty Clinical Trials

Silicone Arthroplasty vs. Arthrodesis in the Distal Interphalangeal Joint

Start date: June 2012
Phase: N/A
Study type: Interventional

The operational and favored standard therapy for the treatment of osteoarthritis in the distal interphalangeal joint is the arthrodesis, in which a titanium screw is used. Arthrodesis shows in the most cases the complete reduction of osteoarthritis pain and low loss of function. But restrictions are reported in fine motor skills. The operation with silicone arthroplasty is similar. As an implant, a silicone joint is used, which has been sufficiently tested at the metacarpophalangeal joint and interphalangeal joint. The advantage of arthroplasty is the function obtained in the distal interphalangeal joint and the resulting improved fine motor skills.

NCT ID: NCT01249612 Terminated - Arthroplasty Clinical Trials

Knee Joint Icing and Knee-extension Strength

IS
Start date: April 2010
Phase: Phase 1
Study type: Interventional

With this study the investigators wish to (1) investigate the acute effect of knee joint icing on knee-extension strength shortly after total knee arthroplasty (TKA); and (2) investigate the acute effect of knee joint icing on knee pain, knee joint circumference and functional performance shortly after TKA.

NCT ID: NCT00683267 Terminated - Arthroplasty Clinical Trials

Efficacy and Safety Study of 4975 in Patients Undergoing Total Hip Replacement

Start date: September 2007
Phase: Phase 2
Study type: Interventional

Evaluate the efficacy, safety and tolerability of a single intraoperative dose of 4975 in patients undergoing total hip replacement

NCT ID: NCT00364533 Terminated - Arthroplasty Clinical Trials

A Study to Evaluate the Effectiveness and Safety of Tapentadol(CG5503) in the Treatment of Acute Pain After Hip Replacement Surgery Compared With Oxycodone and Placebo Followed by a Voluntary Open-Label Extension For Safety

Start date: October 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to test in patients who have had hip replacement surgery the effectiveness (level of pain control) and the safety of 3 different dose levels of CG5503 compared with placebo and with 10-mg oxycodone during the 72-hour double-blind period and to assess the safety of the drug for 9 days after patients completed the double blind period.