Development of a screening tool for outcome related risk factors in patients receiving total hip or knee arthroplasty.

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00011803

Enrollment

300

Registered

2017-06-01

Start date

2017-06-01

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

M17.0 M16.0

Interventions

Group 1: Patients after knee or hip arthroplasty, Screening tool on satisfaction as well as general and psychological variables preoperative, 1 week postoperative and 4 weeks postopratives

Eligibility

Sex/Gender

All

Age

18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Implantation primary hip or knee arthroplasty

Exclusion criteria

Exclusion criteria: revisions, infections

Design outcomes

Primary

Measure	Time frame
Development of a sreening tool for outcome individual risk factors in patients receiving total hip or knee arthroplasty. Preoperative, 1 week postoperatively, 4 weeks postoperatively	—

Secondary

Measure	Time frame
Development of a screening method for postoperative functional limitations Implantation of a hip or knee arthroplasty.	—

Countries

Germany

Contacts

Public ContactStephanie Schmitz

Asklepios Klinik Bad Abbach

s.schmitz@asklepios.com09405/184878

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026