Quality of life after bone and joint infectio

Recruiting

• Conditions: T84.5; T84.6; Infection and inflammatory reaction due to internal joint prosthesis; Infection and inflammatory reaction due to internal fixation device [any site]

• Registration Number: DRKS00025492
• Lead Sponsor: niversitätsklinikum Regensburg

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2023-11-02
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 90

Inclusion Criteria

Patients with verified osteomyelitis, periprosthetic infection, or fracture-associated infection requiring surgical treatment.

Exclusion Criteria

Psychological disorders according to ICD-10 Chapter F.

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary efficacy endpoint is the mental component summary and physical component summary of quality of life assessed by the 36-Item Short Form Health Survey (SF-36), EQ-5D and ISR scores after 12 months.

Secondary Outcome Measures

Name	Time	Method
Secondary outcomes include the mental component summary and physical component summary scores of the SF-36, EQ-5D and ISR scores at 6 months and 24 months.