The Effect of RF Genicular Nerve Block Applied in the Preoperative Period on Fast-track Total Knee Arthroplasty

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age40-85
SponsorPamukkale University

About this trial

In our study, investigators plan to compare the preoperative RF and genicular nerve ablation approach in patients who underwent TKA(Total Knee Arthroplasty) using the Fast-Track protocol in terms of meeting postoperative pain, function and early discharge criteria.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Being between the ages of 40 and 85,

Being able to understand verbal and written information given in Turkish,

Being able to speak and understand Turkish,

Being subjected to unilateral TKA surgery due to the diagnosis of Primary Knee osteoarthritis

Disqualifiers

Patients planned for revision knee prosthesis surgery,

Patients previously diagnosed with psychiatric disorders,

Patients who have undergone major surgery on the extremity where TKA will be applied,

Patients with comorbid diseases such as rheumatoid arthritis or cancer,

Trial population

Inclusion Criteria: * Being between the ages of 40 and 85, * Being able to understand verbal and written information given in Turkish, * Being able to speak and understand Turkish, * Being subjected to unilateral TKA surgery due to the diagnosis of Primary Knee osteoarthritis

Trial design

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

  • Genicular nerve Radiofrequency Ablation block

    Procedure/Surgery

    Genicular nerve Radiofrequency Ablation block

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: TKA with radiofrequency ablation genicular nerve block1 intervention
Group B: TKA without nerve block0 interventions

Trial outcomes

Primary outcomes

1

Pain preoperative

Visual Analog Scale used to assess pain

Time frame
Baseline (preoperatively)
2

Pain postoperative 1

Visual Analog Scale used to assess pain

Time frame
at postoperative sixth weeks
3

Pain postoperative 2

Visual Analog Scale used to assess pain

Time frame
at postoperative twelfth weeks
4

Knee Range of Motion preoperative

Digital goniometer used to assess knee range of motion

Time frame
Baseline (preoperatively)

Secondary outcomes

1

Length of operation time

Length of operation time is measured in minutes during the surgery

Time frame
the surgery
2

Amount of blood loss

Amount of blood loss is measured from the suction drainage (unit-milliliters)

Time frame
through study completion, an average of 1 year
3

postoperative component alignments

Long leg radiographs of the patients are evaluated postoperatively by using a digital orthopedic templating software-Materialise OrthoView (OrthoView version 7, Materialise HQ, Technologielaan 15 3001 Leuven, Belgium).

Time frame
through study completion, an average of 1 year

Other outcomes

Sponsors and contacts

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