Development of a screening tool for outcome relatedrisk factors in patients receiving total hip or kneearthroplasty.

Recruiting

• Conditions: M17.0; M16.0; Primary gonarthrosis, bilateral; Primary coxarthrosis, bilateral

• Registration Number: DRKS00011803
• Lead Sponsor: Asklepios Klinik Bad Abbach

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2017-06-01
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 300

Inclusion Criteria

Implantation primary hip or knee arthroplasty

Exclusion Criteria

revisions, infections

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Development of a sreening tool for outcome individual risk factors in patients receiving total hip or knee arthroplasty.<br><br>Preoperative, 1 week postoperatively, 4 weeks postoperatively

Secondary Outcome Measures

Name	Time	Method
Development of a screening method for postoperative functional limitations<br>Implantation of a hip or knee arthroplasty.