Knee Disease Clinical Trial
Official title:
Partial Versus Total Knee Replacement in Bicompartmental Gonarthrosis (Medial and Patellofemoral): Prospective Functional Assessment Study
The study is, in accordance with current legislation, definable as a prospective single-center interventional randomized study. The aim of the study is to evaluate the post-operative recovery of the group A patient undergoing the partial knee replacement surgical procedure compared to the group B patient undergoing the total knee replacement surgical procedure through clinical/functional scores. The primary outcome is evaluate the difference in score of the KSS questionnaire, at 1 month after surgery, completed by the patient of group A compared to the patient of group B. The population consists of 48 adult patients with gonarthrosis divided into two groups: 24 patients Group A experimental group: partial denture surgical procedure 24 patients Group B control group: total denture surgical procedure with patellar resurfacing
The medial unicompartmental prosthesis procedure associated with patellofemoral is reserved for active patients suffering from bicompartmental gonarthrosis in which total knee replacement is to be avoided. The advantage for the patient, compared to total prosthesis surgery, consists in the less invasive nature of the surgical gesture, in the total preservation of the cruciate ligaments and the external compartment and therefore of the native joint biomechanics with the possibility of remote revision with total prosthesis from first implant. Patients keep "their knee" which is coated and not replaced with advantages in terms of joint feedback and functionality in daily activities and sports practices. This study aims to compare two groups of patients suffering from bicompartmental gonarthrosis (medial and patellofemoral gonarthrosis): Group A undergoing a bicompartmental prosthesis surgical procedure; Group B undergoing a total denture surgical procedure with patellar resurfacing. The two groups will be evaluated with clinical and functional scores aimed at evaluating the outcome in the two surgical procedures. The number and type of exams are as follows: - Randomization to Group A or Group B (ad hoc) - Knee replacement surgery (as usual) - Compilation of KSS questionnaire at 1, 2, 6, 12 months of follow-up with clinical and functional scores (as a matter of practice) - Questionnaires and scales (WOMAC, Tegner, VAS and patient satisfaction) at 2, 6, 12 months post intervention (as a matter of practice) - Recording of any adverse events at 1, 2, 6, 12 months after surgery (as a matter of practice) ;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Terminated |
NCT04578951 -
Measurement of the Quality of Life in Patients Operated With a Total Knee Prosthesis (TKA) From the FHK® Range.
|
||
| Recruiting |
NCT05566561 -
Para-sartorial Compartment Block in Knee Surgery
|
N/A | |
| Completed |
NCT05533970 -
Ultrasound-guided H-FICB for Arthroscopic Knee Surgery： What is the Optimal Dose of Dexmedetomidine?
|
N/A | |
| Completed |
NCT04648072 -
How Does the Addition of Adductor Canal Block to Local Infiltration Affect Recovery in Patients Undergoing Total Knee Arthroplasty? A Feasibility Study.
|
N/A | |
| Completed |
NCT05621161 -
ESPB vs FICB for Pain Management Following Total Hip Prosthesis Surgery
|
N/A | |
| Completed |
NCT04388111 -
Intraosseous Morphine in Primary TKA
|
Phase 4 | |
| Not yet recruiting |
NCT06284824 -
Comparison of Two Robotic-Assisted Total Knee Arthroplasty Systems
|
N/A | |
| Not yet recruiting |
NCT05749965 -
Results of Unicompartmental Knee Arthroplasties in Patients Beyond Historical Indications (PUCIL)
|
||
| Not yet recruiting |
NCT06144099 -
Prothrombin Complex Concentrate vs Fresh Frozen Plasma in Goal-directed Bleeding Management in Non-cardiac Surgery
|
Phase 4 | |
| Active, not recruiting |
NCT05448742 -
Biplanar PSI Slope-reducing MOWHTO With Tibial Tuberosity Serving as Hinge Axis: Cadaveric Study
|
N/A | |
| Not yet recruiting |
NCT05889286 -
F18-MHF: Orthopedic Implants-Associated Infection Detection
|
||
| Active, not recruiting |
NCT06087562 -
iPACK Block for Total Knee Arthroplasty
|
Phase 4 | |
| Recruiting |
NCT04821154 -
Persona Revision Knee System Outcomes
|
||
| Recruiting |
NCT05385393 -
Functional Outcomes and the Restoration of Range of Motion After the Arthroscopic Complete Posterior Knee Capsulotomy in Patients With Extension Deficit of the Knee
|
N/A | |
| Recruiting |
NCT04422119 -
Standard Dressing Versus Moist Dressing in the Course of the Postoperative Wound in Patients With Knee Prosthesis
|
N/A | |
| Recruiting |
NCT04321629 -
Knee Arthritis Treatment With Autologous Fragmented Adipose Tissue and PRP - Comparison of Two Treatment Methods
|
Phase 2 | |
| Active, not recruiting |
NCT04872855 -
Observational Study to Evaluate Clinical Performance and Safety in Total Knee Arthroplasty
|
||
| Completed |
NCT05669066 -
Meditation and Opioid Consumption in Total Joint Replacement Patients Undergo Primary Total Hip and Knee Replacement
|
N/A | |
| Terminated |
NCT04650594 -
Functional Outcomes of Knee Protheses for Malignant Tumours of Bone
|
N/A | |
| Active, not recruiting |
NCT04221581 -
Study Conducted on Patients Operated With a FHK ASYMETRIQUE to Confirm Security and Performance of the Device
|