Post-market surveillance study to prove the safety and performance of Vanguard PS RP
Not Applicable
- Conditions
- Knee joint deseases
- Registration Number
- JPRN-UMIN000023965
- Lead Sponsor
- Zimmer Biomet G.K.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
1)Infection, sepsis, and osteomyelitis 2)Sensitivity for material of the investigational implant 3)Uncooperative patient or patient with neurologic disorders who are incapable of following directions 4)Pregnancy
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Implant survivorship at 10 years postoperatively
- Secondary Outcome Measures
Name Time Method Safety, Pain and functional performance of the knee