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Recruiting Observational

Study of the Clinical and Radiographic Results of a Fixed Polyethylene Posteriorly Stabilized Cemented Total Knee Prosthesis With a Minimum Follow-up of 1 Year.

NCT07313449 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2025-01-31
Last updated
2026-01-02

Condition(s) studied

Hip Osteoarthritis

Study summary

The knee replacement market is experiencing constant growth. Alongside this growth, there is also an increasing interest in customizing implantation based on specific phenotypes to restore the morphology of the native knee. For example, in the last five years, 2019 publications on knee prosthesis alignment have been identified on PubMed.

It seems worthwhile to study and analyze the performance of the prosthesis used in the Orthopedic Surgery Department of the Strasbourg University Hospitals (HUS) and to compare it with results from the literature.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adult patient * Patient who underwent total knee replacement (TKR) between January 2013 and December 2024 * Patient who underwent an Anatomic, Amplitude, posteriorly stabilized, fixed polyethylene, cemented TKR * Patient operated on by Professor F. Bonnomet * Available radiological data: preoperative, immediate postoperative, and postoperative at a minimum of 1 year follow-up Exclusion Criteria: \- Revision of the arthroplasty during the study follow-up period for a cause not investigated in the study

Primary outcome measure(s)

  • IKS / KSS (Knee Society Score) — Up to 12 months
    The classic IKS (often called KSS) has 2 separate scores, each out of 100 points: 1. Knee Score (Objective / Clinical) - 0 to 100 Assesses the knee itself: * Pain (0-50) * Range of motion (0-25) * Stability (0-25) 2. Function Score - 0 to 100 * Assesses patient function: * Walking distance (0-50) * Stair climbing (0-50) Interpretation (commonly used): * 80-100: Excellent * 70-79: Good * 60-69: Fair * \< 60: Poor

Trial sites (1)

FacilityCityRegionStatus
Service de Chirurgie Orthopédique et de Traumatologie du Membre Inférieur - CHU de Strasbourg - France Strasbourg France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07313449 on ClinicalTrials.gov ↗ ← All trials in France