ong-term outcomes of total hip and knee arthroplasties.
Recruiting
- Conditions
- osteoarthritis, arthritis, total hip prosthesis, total knee prosthesis
- Registration Number
- NL-OMON22630
- Lead Sponsor
- MC, LeidenRijnland Ziekenhuis, LeiderdorpDiaconessenhuis, LeidenGroene hart ziekenhuis, LeidenLange land ziekenhuis, Zoetermeer
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 4500
Inclusion Criteria
1. All patients who are scheduled for primary total hip or total knee surgery or revision surgery;
2. Are able to complete questionnaires, either on paper or electronically;
Exclusion Criteria
1. No informed consent signed;
2. Insufficient Dutch language skills;
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Knee or hip functioning (HOOS/KOOS);<br /><br>2. Physical activity (SQUASH questionnaire, accelerometer);<br /><br>3. Work status;<br /><br>4. Quality of life (SF-12 and EQ-5D);<br /><br>5. Patient satisfaction;<br /><br>6. Health care usage;<br /><br>7. Radiological outcome (post-operative femorotibial angle (knee) and alignment of the stem and inclination of the cup (Hip) and post-operative complications.
- Secondary Outcome Measures
Name Time Method 1. Sociodemographic characteristics (age, sex);<br /><br>2. Comorbidities (comorbidity questionnaire, Charnley classification and ASA classification);<br /><br>3. Frailty (>70 years of age: Groningen Frailty Index);<br /><br>4. Pre-operative use of pharmacological and non-pharmacological treatment for hip or knee pain;<br /><br>5. Outcome expectations (the New York Hospital for Special Surgery Questionnaire);<br /><br>6. Preoperative radiographic damage (Kellgren score, Femorotibial angle and alignment of the stem and inclination of the cup) and hand grip strength.