Heidelberg Registry for Hip and Knee Joint Implants and Revisions

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Hospital Heidelberg

About this trial

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

This trial does not accept healthy volunteers

Qualifiers

All patients undergoing hip or knee arthroplasty at our institution

All patients undergoing revision surgery following hip oder knee arthroplasty

Disqualifiers

Lack of prospective consent for study participation

Lack of capacity to provide informed consent

Minor status (underage)

Trial population

All patients undergoing surgery at the Department of Orthopedic Surgery, Heidelberg University Hospital.

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Survival analysis with the endpoint revision for any reason

Kaplan Meier Analysis

Time frame
Preoperative, 1 year, 3 years, and every 5 years

Secondary outcomes

1

Knee Society Score

The Knee Society Score (KSS) provides a 0 to 100 score measuring function, pain, and range of motion in the knee before and after surgery. A score of 0 indicates the worst outcome, while a score of 100 indicates the best outcome.

Time frame
preoperative, 1 year, 3 years and every 5 years
2

Forgotten Joint Score

The Forgotten Joint Score assesses how aware the patient is of their joint in everyday life. A score of 0 is the worst (always aware) while a score of 100 is the best (the patient is so comfortable, they forget that the joint was replaced).

Time frame
preoperative, 1 year, 3 years and every 5 years
3

Oxford Knee/Hip Score

The Oxford Knee Score (OKS) provides a 0 to 48 score measuring function, pain, and range of motion in the knee before and after surgery. A score of 0 indicates the worst outcome, while a score of 48 indicates the best outcome

Time frame
preoperative, 1 year, 3 years and every 5 years
4

Harris Hip

This survey assesses pain, deformity, and range of motion of the hip. A score of 0 indicates the worst outcome and 100 indicates the best.

Time frame
preoperative, 1 year, 3 years and every 5 years

Other outcomes

Sponsors and contacts

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