Comparison of Two Different Regional Anesthetic Methods in Total Knee Arthroplasty Patients

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorSB Istanbul Education and Research Hospital

About this trial

Total Knee Arthroplasty patients are among the orthopedic cases that experience severe postoperative pain. In these cases, pain must be controlled. If pain is not controlled, early mobilization cannot be achieved. This can result in delayed physical therapy, prolonged hospital stays, the development of nosocomial infections, and impaired cognitive function. All of these factors contribute to increased patient care costs. Multimodal analgesia methods are used to control this pain. One of these methods is peripheral nerve blocks. Peripheral nerve blocks provide pain control and reduce the likelihood of opioid use and related side effects such as nausea, vomiting, and constipation. Current studies recommend Adductor Canal Blocks and iPACK (space between the popliteal artery and the posterior knee capsule) blocks for Total Knee Arthroplasty patients. In addition, studies are also being conducted on the application of the Suprainguinal Fascia-Iliaca Block in Total Knee Arthroplasty patients. The differences in postoperative analgesic effects between these methods are a matter of interest. No study has been conducted comparing the effects of these two approaches, which are routinely applied in our clinic and comply with guidelines, on the postoperative stress response. Regional anesthesia provides adequate pain control and has a positive effect on the stress response. The investigators aim to see a similar effect in peripheral nerve blocks. Therefore, comparing the methods that mentioned will contribute to the literature. In this study, the effects of these two different approaches on postoperative stress response and analgesic efficacy will be compared in terms of patients' postoperative opioid consumption, pain at rest and with movement, time to first analgesic need and development of motor block. IL-6 and CRP values will be examined pre-operatively and post-operatively to measure the effects on the stress response.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients undergoing total knee arthroplasty

Patients aged 18-75

Patients with ASA I-II-III

Disqualifiers

Coagulation disorders

Allergy to local anesthetics

Liver and renal failure

Alcohol and drug addiction

Trial design

Design model

Parallel

Treatments tested in this trial

  • Ultrasound Guided Suprainguinal Fascia Iliaca Block

    Procedure/Surgery

    Ultrasound Guided Suprainguinal Fascia Iliaca Block, 30 ml Bupivacain %0,25

  • Ultrasound Guided Adductor Canal Block

    Procedure/Surgery

    Ultrasound Guided Adductor Canal Block, 15ml Bupivacain %0,25

  • Ultrasound Guided iPACK Block

    Procedure/Surgery

    Ultrasound Guided iPACK Block, 15ml Bupivacain %0,25

Treatment groups

52 Participants
are divided into 2 treatment groups
Group A: Ultrasound Guided Fascia Iliaca BlockActive comparator 1 intervention
Group B: Ultrasound Guided Adductor Canal Block + iPACK BlockActive comparator 2 interventions

Trial outcomes

Primary outcomes

1

Cumulative opioid consumption

Tramadol consumption will be recorded for 24 hours.

Time frame
24 hours

Secondary outcomes

1

Numeric rating scale for pain

Variations in the Numeric Rating Scale (NRS) scores, both at rest and during movement, will be documented at specific time points (End of the surgery, Post-operative 6th, 12th and 24th hour). The NRS is a simple, single-dimensional tool used to assess pain intensity in adult patients. It is a numeric adaptation of the Visual Analog Scale (VAS), where individuals are asked to choose an integer between 0 and 10 that best represents their pain level. A score of '0' corresponds to "no pain," while '10' indicates the "worst imaginable pain" or "pain as severe as possible.

Time frame
Up to 24 hours
2

Time to first postoperative analgesic requirement

The time to first postoperative analgesic requirement was recorded.

Time frame
Up to 24 hours
3

Postoperative quadriceps muscle strength

Muscle strength assessment will be performed using the Modified Bromage Scale. (End of the surgery, Post-operative 6th, 12th and 24th hour) Grade 0: No motor block; the patient is able to fully flex the hip and knee. Grade 1: Partial motor block; the patient is able to move the knee and foot but is unable to lift the extended leg. Grade 2: Nearly complete motor block; the patient is unable to flex the knee and can only move the foot. Grade 3: Complete motor block; the patient is unable to move the ankle or the great toe.

Time frame
Up to 24 hours
4

Incidence of postoperative nausea and vomiting

Opioid side effects were recorded.

Time frame
Up to 24 hours

Other outcomes

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