Instrumented Hip Joint Prostheses: Load measurements in patients using an instrumented endoprosthesis
- Conditions
- M16Coxarthrosis [arthrosis of hip]
- Registration Number
- DRKS00000563
- Lead Sponsor
- Julius Wolff Institut, Berlin Institute of Health at Charité - Universitätsmedizin Berlin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
Only patients needing a conventional total hip prosthesis.
Exclusion Criteria
Excludes are all patients with active implants (eg cardiac pacemakers).
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperatively, even during the stay in hospital will be conducted during regular physiotherapy about 2x weekly measurements. After the hospital stay, these in the course to 6 Months after surgery about a month later in 1x and made every six months.
- Secondary Outcome Measures
Name Time Method In the course of the study will be conducted with the patients gait analysis. For this purpose, the patient receives reflective markers taped to the skin. The movement of the markers is in various activities through an infrared camera system recorded and then allowing the movement in the form of velocity of the segments and joint angles can be analyzed. Force plates in the floor to allow the simultaneous recording of ground reaction forces. This synchronous motion and force data recorded are the basis to determine with a musculoskeletal model, the calculation of internal stress of the musculoskeletal system.