Oyonnax

Researchers are gathering long-term real-life clinical data on patients who have undergone hip joint replacement or repair using medical devices from FH ORTHO Company. This study focuses on the clinical safety and performance of these devices when used as approved, including different versions and combinations of implants used in arthroplasty and trauma repair. The study operates as a dynamic cohort, allowing new participants to join to replace those who leave early. The intervention involves hip surgery using one or more FH ORTHO Company devices, as applied by surgeons at participating centers. The study includes patients who have these devices implanted in accordance with approved instructions. Data collection is supported by electronic systems for surgeons (electronic Case Report Form) and patients (Electronic Patient Reported Outcome via phone, tablet, or computer). Participants will be followed for up to 15 years to monitor the survival rate and revision of the medical devices. The study collects ongoing clinical data through patient and surgeon reports, focusing on device performance and safety over the long term. Consent and local regulations regarding patient inclusion apply, with some countries requiring social insurance for participation.