Heidelberg Registry for Hip and Knee Joint Implants and Revisions

NCT06850818 · tracked via the Priya Life Science Germany tracker

Sponsor

University Hospital Heidelberg

Phase

Observational

Started

2007-01-01

Last updated

2026-06-11

Condition(s) studied

OsteoarthritisArthroplasty

Study 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

Sex

ALL

Min age

18 Years

Max age

—

Healthy volunteers

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)

Primary outcome measure(s)

Survival analysis with the endpoint revision for any reason — Preoperative, 1 year, 3 years, and every 5 years
Kaplan Meier Analysis

Trial sites (1)

Facility	City	Region	Status
University Hospital Heidelberg	Heidelberg	Baden-Wurttemberg	Recruiting

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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 NCT06850818 on ClinicalTrials.gov ↗ ← All trials in Germany