Investigation of patient satisfaction following use of the VERASENSE sensor to monitor operative contact pressure during TKA
Not Applicable
- Conditions
- Osteoarthritis Rheumatoid Arthritis Osteonecrosis
- Registration Number
- JPRN-UMIN000039794
- Lead Sponsor
- Fujita health university
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Not provided
Exclusion Criteria
Patients with severe systemic disorders (heart, lung, or cerebrovascular diseases, or psychiatric disorders) and other patients the study investigator and/or study doctor considers as not appropriate
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method