A comparative study of the results of using 3 suture techniques in total knee joint replacement surgeries
Not Applicable
Recruiting
- Conditions
- total knee joint replacement surgerie.
- Registration Number
- IRCT20230506058104N1
- Lead Sponsor
- Hamedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 96
Inclusion Criteria
Adult patients (18 years or older)
Having a signed informed consent form
Patients who are candidates for total knee replacement
Exclusion Criteria
History of keloid scar formation
Long-term use of corticosteroids
Uncontrolled diabetes (Fasting blood sugar 200 mg/dL or more)
Previous knee surgery
Hypoalbuminemia Less than 5.3 mg/dL
Anemia (Hemoglobin less than 10 mg/dL)
Inflammatory joint disease (rheumatoid arthritis-psoriatic arthritis-bursitis...)
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Scar in patient and surgeon scar evaluation questionnaire. Timepoint: 2 weeks-6 weeks-3 months. Method of measurement: Patient and surgeon scar evaluation questionnaire (PoSAS) - VAS surgeon satisfaction evaluation scale.
- Secondary Outcome Measures
Name Time Method