Synovitis after Total Knee Arthroplasty - longitudinal study
Not Applicable
Recruiting
- Conditions
- osteoarthritis
- Registration Number
- JPRN-UMIN000041036
- Lead Sponsor
- Orthopaedics surgery, Kochi University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 45
Inclusion Criteria
Not provided
Exclusion Criteria
patients having history of pyogenic arthritis of the knee, Lumber spine stenosis, postoperative neuropathic pain in wound of TKA, and post operative infection.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method pain scale(pain VAS) in postoperative six month
- Secondary Outcome Measures
Name Time Method postoperative alignment of implants, knee instability, age at the surgery, preoperative PD total score, and CRP of synovial fluid.
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular pathways drive synovitis development after TKA in osteoarthritis patients?
How does synovitis incidence in JPRN-UMIN000041036 compare to standard-of-care outcomes for osteoarthritis post-TKA?
Are specific biomarkers predictive of synovitis progression in osteoarthritis patients following TKA?
What adverse events are reported in patients with synovitis after TKA in this observational study?
What drug classes or combination therapies are being explored for synovitis management in post-TKA osteoarthritis patients?