Knee Arthropathy
Conditions
Brief summary
The purpose of the study is the rate of return to sport (regardless of the sport envisaged) after a minimum of 3 years after total knee prosthesis.
Detailed description
This is an ambispective, comparative study of three cohorts, non-randomized, open, monocentric, relating to the return to sport of patients who have benefited from one of the three designs of prostheses under study (medial pivot, medial bearing and cruciate retaining) after total knee prosthesis. Patients who received a total knee prosthesis with medial pivot, medial bearing and cruciate retaining prosthesis between 2018 and 2020 will be called by the investigator, and the study will be offered to them (D-3 to D0). The investigator will explain the study to the patient, send him the information note electronically and answer all his questions about the study. If the patient agrees to participate after a reflection period, the inclusion (D0) will be documented in the medical file, and the patient will be assessed the same day by telephone using the assessments set up in the study, except for the questionnaires on his functional and physical abilities that will be sent to him electronically. The patient will return his answers to the questionnaires on this same email address or by telephone according to his preference. A secure and unique email address will be created by the principal investigator for the purposes of the study and for use strictly specific to the study, in the investigating center.
Interventions
OTHERtotal knee prosthesis
Comparison of three cohorts on the return to sport of patients after total knee prosthesis according to the type of prosthesis
Sponsors
Euraxi Pharma
GCS Ramsay Santé pour l'Enseignement et la Recherche
Study design
Observational model
COHORT
Time perspective
OTHER
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
* First total knee prosthesis between 2018 and 2020; * Conventional alignment technique using the same surgical technique for total knee prosthesis; * Placement of a medial pivot prosthesis (Evolution®), mobile bearing (SCORE® Amplitude) or traditional cruciate retaining prosthesis (Stryker® Triathlon); * Affiliation to a social security scheme; * Patient having been informed and having given his oral non-objection
Exclusion criteria
* Bilateral total knee prosthesis; * Medical history of revision of Total Knee Prosthesis; * Articulation malformation of the lower limbs; * Having undergone revision surgery; * Inability to understand information related to the study for linguistic, psychological, cognitive reasons; * Patient under legal protection, or deprived of liberty by judicial or administrative decision.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| rate of return to sport | 3 years | rate of return to sport after a minimum of 3 years after total knee prosthesis |
Countries
France
Outcome results
None listed