Registry for hip and knee joint implants and revisions

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The Endoprosthesis Registry Heidelberg (EPR-HD) systematically collects and analyzes data from patients undergoing primary or revision surgeries of artificial hip and knee joints. It aims to evaluate long-term outcomes, complication rates, implant survival, and functional results associated with joint replacement procedures. By gathering comprehensive clinical data, the registry seeks to improve understanding of patient outcomes and identify factors influencing implant success, ultimately supporting evidence-based improvements in surgical techniques and patient care. Data will be collected at multiple time points during routine clinical follow-up at Heidelberg University Hospital.

Why it matters

Who can join: the full rules

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)

Where it's running

• University Hospital Heidelberg
  Heidelberg, Baden-Wurttemberg, Germany Recruiting

Study contacts

• Study coordinator: Mustafa Hariri, MD
• Email: mustafa.hariri@med.uni-heidelberg.de
• Phone: 004962215635652

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.