Heidelberg Registry for Hip and Knee Joint Implants and Revisions
Trial Parameters
Brief Summary
The Endoprosthesis Registry Heidelberg (EPR-HD) is a clinical registry designed to systematically collect and analyze data from patients undergoing primary implantation or revision surgery of artificial hip and knee joints. The main objective of the registry is to evaluate long-term outcomes, complication rates, implant survival, and functional results associated with joint replacement procedures in patients with various hip and knee joint pathologies. By gathering comprehensive clinical data, EPR-HD aims to improve the understanding of patient outcomes after endoprosthetic procedures, identify potential factors influencing implant success, and support evidence-based improvements in surgical techniques and patient care. The registry includes adult patients treated at Heidelberg University Hospital, with data collected at multiple time points during routine clinical follow-up. This registry will contribute to the optimization of joint replacement strategies and promote high-quality patient care.
Eligibility Criteria
Inclusion Criteria: * All patients undergoing hip or knee arthroplasty at our institution * All patients undergoing revision surgery following hip oder knee arthroplasty Exclusion Criteria: * Lack of prospective consent for study participation * Lack of capacity to provide informed consent * Minor status (underage)