Arthroplasty Clinical Trial
Official title:
Gait Analysis, Stair Performance and CT-based Micromotion Analysis in Robotic Assisted Total Knee Arthroplasty Comparing Bi-cruciate Retaining vs Cruciate Retaining Implants: A Single Centre Patient-blinded Randomized Controlled Trial
The goal of this clinical trial is to compare the function of the knee after retaining or sacrificing the anterior cruciate ligament in robotic assisted knee arthroplasty. The main questions it aims to answer are: Does retaining the anterior cruciate ligament improve postoperative gait? Participants will perform - Gait analysis - Stair performance test - CT based Micromotion analysis of the implant micromovement
A randomized controlled clinical trial intended to compare walking function and movement of the prosthesis after robot-assisted knee replacement surgery with two knee replacement designs; One prosthesis is preserving the anterior cruciate ligament (Smith+Nephew Journey II XR) and the other is sacrificing the anterior cruciate ligament (Smith+Nephew Jourrney II CR). It is common to remove anterior cruciate ligament during knee replacement surgery. There is speculation about this weakens the balance in the operated knee and whether this can explain some of the problems that up to 20% experience after knee replacement surgery. Preservation of the anterior cruciate ligament during knee replacement surgery may provide a more natural movement and better balance in the operated knee, and this in turn could provide increased patient satisfaction. Previous studies have shown that knee replacement surgery where the anterior cruciate ligament is preserved has an increased incidence of per- and postoperative complications and reduced implant survival. Robot assisted navigation in knee arthroplasty surgery has shown the possibility of increased precision and accuracy when implanting the knee prostheses, and therefore might provide increased satisfaction when performing elective knee prosthetic surgery with robotic assistance and at the same time preserving the anterior cruciate ligament without an increased risk of complications. In this study, postoperative function is assessed by looking at whether the walking pattern has normalized. Gait analyses with comparison of the two groups is carried out both before surgery and 2, 6 and 12 months after surgery. Primary endpoint is self-selected walking speed at 12 months follow-up. Secondary endpoints include other gait analysis parameters, result of stair test, as well as patient-reported pain, satisfaction and function (NRS, EQ-5D-5L, KOOS-PS, IKSS, FJS-12), knee mobility, stability, and hip-knee-ankle angle. Complications related to the surgery or the course afterwards is noted. The study will also compare the movement of the prosthetic components in relation to the skeleton over a period of 2 years using a CT based micro motion analysis method (CT-RSA) making it possible to assess implant migration over time. Increased movement can predict early loosening of the prosthesis. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Not yet recruiting |
NCT06323980 -
INHANCE Stemless Reverse Shoulder IDE
|
N/A | |
Completed |
NCT00762944 -
Total Temporomandibular Joint Replacement System Post Approval Study
|
||
Not yet recruiting |
NCT05015101 -
Evaluation of the Clinical and Radiological Outcome of Uncemented Femoral Stems According to Their Proximal Coating
|
||
Completed |
NCT02554149 -
Radiological Measurement of Femoral Stem Version Using Lateral Decubitus Method: A Prospective Study
|
N/A | |
Terminated |
NCT02713906 -
Materialise X-ray Knee Guides for Total Knee Arthroplasty
|
N/A | |
Recruiting |
NCT02828293 -
Understanding GMK Sphere Implant Tibiofemoral Kinematics by Means of Dynamic Videofluoroscopy
|
||
Completed |
NCT02829866 -
AMIStem-H Radiographic Analysis
|
||
Terminated |
NCT00683267 -
Efficacy and Safety Study of 4975 in Patients Undergoing Total Hip Replacement
|
Phase 2 | |
Completed |
NCT04516239 -
Comparison of Metal on Metal Total Hip Arthroplasty and Metal on Metal Total Hip Resurfacing.
|
Phase 4 | |
Recruiting |
NCT04480320 -
Sonography-guided Pericapsular Never Group Block for Hip Arthroplasty
|
N/A | |
Not yet recruiting |
NCT04906681 -
Implementation of a Rehabilitation Technology in Orthopedic and Neurological Rehabilitation to Increase Therapy Dosage: an Exploratory Study
|
Phase 1/Phase 2 | |
Completed |
NCT04403919 -
Knotless Suture in Revision Total Joint Arthroplasty
|
N/A | |
Completed |
NCT03132831 -
Influence of the Operative Day on the Average Duration of Stay in Primary Hip and Knee Replacements
|
||
Active, not recruiting |
NCT03339557 -
Comparison of Three Knee Replacements
|
N/A | |
Active, not recruiting |
NCT02578446 -
Uncemented Tritanium Compared With Cemented Metal-backed Tibia Components in Total Knee Replacement
|
N/A | |
Not yet recruiting |
NCT00756483 -
Stability Plus - Outcomes From Extended Continuum of Care
|
N/A | |
Terminated |
NCT00364533 -
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
|
Phase 3 | |
Terminated |
NCT04089371 -
A Post-Market Clinical Evaluation of the ReUnion Reversible Fracture (RFX) System
|
||
Completed |
NCT05248854 -
Effects of Sensorimotor and Core Stabilization Exercises After Total Knee Arthroplasty
|
N/A | |
Not yet recruiting |
NCT02465684 -
Effect of Tourniquet on UKA
|
N/A |