About this trial
The study is a prospective observational study designed to determine the effects of central sensitization on pain and functional status of patients before and after total knee joint replacement surgery.
The aim of this study is to evaluate whether there is a difference in preoperative and postoperative pain and functional status between patients with and without central sensitization with knee osteoarthritis.
When the literature was reviewed, it was seen that central sensitization was one of the important mechanisms that caused pain in knee osteoarthritis, and it was determined that this had negative consequences in terms of postoperative pain and improvement in functional status. In this study, the effect of central sensitization on the results will be investigated by evaluating pain and functional status before and after knee total joint prosthesis in two groups of knee osteoarthritis patients, with and without central sensitization, and by comparing the groups.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Diagnosis of primary knee osteoarthritis
Planning for total joint replacement surgery for the knee
Being between the ages of 60-75
Disqualifiers
Having secondary knee osteoarthritis
Planning for knee total joint prosthesis revision
Having uncontrolled systemic disease (such as diabetes mellitus, hypertension, thyroid disease)
Having neuromuscular disease
Trial population
The study population consists of patients who were planned to have total knee arthroplasty for primary knee osteoarthritis
Trial design
Cohort
Prospective
Treatments tested in this trial
Total knee arthroplasty
Procedure/SurgeryPatients already admitted for total knee arthroplasty for knee osteoarthritis will have the procedure as planned
Treatment groups
Trial outcomes
Primary outcomes
Knee pain
Knee pain will be assessed with numerical rating scale, where the patients rate their pain on a scale from 0 to 10 where 0 means no pain and 10 means the most severe pain they can imagine.
Secondary outcomes
Functional Status
Functionality of the patients will be assessed with WOMAC (Western Ontario and McMaster Universities Osteoarthritis Index). Responses are typically rated on a scale from 0 (none) to 4 (extreme). Higher scores indicate greater impairment.
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: