Prospective data collection based on EndoCert questionnaires for the outcomes and quality of life of patients who have undergone arthroplasty – a multicenter study

Recruiting

• Conditions: M16; M17; Coxarthrosis [arthrosis of hip]; Gonarthrosis [arthrosis of knee]

• Registration Number: DRKS00033383
• Lead Sponsor: Orthopädische Klinik und Poliklinik der Universitätsmedizin Rostock

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-01-09
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 1250

Inclusion Criteria

Indication for primary hip arthroplasty
Indication for primary knee arthroplasty
Indication for revision of a hip arthroplasty
Indication for revision of a knee arthroplasty

Exclusion Criteria

Fractures and Tumor Surgeries

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
- Oxford Score (=PROMs)<br>- EuroQol-5D Score (= quality of life)<br>- EndoCert-Riskscore (=PROMs, Net Promoter Score)<br>- Patients' Experience Questionnaire (PEQ=PREMs)<br>- Complications (according to EndoCert), re-interventions<br>- Length of hospital stay

Secondary Outcome Measures

Name	Time	Method
patient-specific risk factors, Pain symptoms, reasons for revision<br>Center comparison