Oyonnax

Researchers are collecting real-life clinical data on patients who have had hip surgery using medical devices from FH ORTHO Company. This study, a Post-Market Clinical Follow-up PMCF observatory, aims to answer specific questions about the safety and performance of these devices when used as intended. It includes patients undergoing hip joint replacement or repair after trauma, covering different device versions and implant combinations. The study monitors patients who have had total hip arthroplasty, revision surgeries, or traumatology-related hip procedures using FH ORTHO devices. Patients will be followed for up to 15 years post-surgery to observe the devices long-term outcomes. Data collection is facilitated through electronic case report forms completed by surgeons and electronic patient-reported outcomes via phone, tablet, or computer. Participants will provide consent and may be monitored through regular follow-up visits and data collection over many years. Researchers will review the survival rate of the medical devices, focusing on revision rates as the main outcome measure. The study includes ongoing monitoring for up to 10 or 15 years, depending on the patients procedure, to gather comprehensive safety and performance information.