Clinical trial of a new silicone mold for dynamic spacer production during knee surgery: a pilot clinical trial study
Not Applicable
Recruiting
- Conditions
- Prosthetic Joint Infection.Infection and inflammatory reaction due to internal joint prosthesisT84.5
- Registration Number
- IRCT20191111045400N2
- Lead Sponsor
- Bojnourd University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 7
Inclusion Criteria
aspiration of infectious synovial fluid from patient (determined by differential count of the number of white blood cells and the percentage of polymorphonuclear leukocytes)
isolation of organism(s) from synovial Fluid of patient
presence of a draining sinus
MRI evidence of a septic arthritis with osteomyelitis
Exclusion Criteria
polyarticular joint involvement
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Physical function. Timepoint: 1 month, 3 months, 6 months and one year after surgery. Method of measurement: They are scored through the WOMAC Score questionnaire and the Oxford Knee Score questionnaire.
- Secondary Outcome Measures
Name Time Method