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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
NameTimeMethod
pain scale(pain VAS) in postoperative six month
Secondary Outcome Measures
NameTimeMethod
postoperative alignment of implants, knee instability, age at the surgery, preoperative PD total score, and CRP of synovial fluid.
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