Evaluation of the Effect of Central Sensitivity on Pain and Functional Status After Total Knee Joint Replacement Surgery

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age60-75
SponsorIstanbul University

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 volunteers

Qualifiers

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

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Total knee arthroplasty

    Procedure/Surgery

    Patients already admitted for total knee arthroplasty for knee osteoarthritis will have the procedure as planned

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: Central Sensitization Group1 intervention
Group B: Non-sensitized Group1 intervention

Trial outcomes

Primary outcomes

1

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.

Time frame
Preoperative, 1 month postoperative and 3 months postoperative

Secondary outcomes

1

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.

Time frame
Preoperative, 1 month postoperative and 3 months postoperative

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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