Pilot study on indication-specific rehabilitation - rehabilitation outcome of thecomorbidities and risk factors for osteoarthritis and influence on knee pain (osteoarthritis) and Cartilage degradatio

Recruiting

• Conditions: patients after total knee replacement; M17; Gonarthrosis [arthrosis of knee]

• Registration Number: DRKS00031387
• Lead Sponsor: udwig Boltzmann Institut für Arthritis und Rehabilitation

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2023-06-21
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 250

Inclusion Criteria

Module 1: Knee pain greater than or equal to 3 (VAS)
Module 2: Follow-up treatment KTEP
Module 3: end-stage OA, patient directly before KTEP
Men not older than 65, women not older than 60

Exclusion Criteria

Cortisone treatment (excl. inhalation), rheumatoid arthritis

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
3 weeks after inpatient rehabilitation (T1):<br>KOOS (knee pain and function), EQ-5D (quality of life), WAI (work ability index), VAS (pain)<br>Blood parameters/cartilage remodeling: blood sampling and ELISA

Secondary Outcome Measures

Name	Time	Method
Follow-up 6 months after inpatient rehabilitation (T2):<br>KOOS (knee pain and function), EQ-5D (quality of life), WAI (work ability index), pain scale 0-10 (pain).