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 volunteersQualifiers
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
Parallel
Treatments tested in this trial
Ultrasound Guided Suprainguinal Fascia Iliaca Block
Procedure/SurgeryUltrasound Guided Suprainguinal Fascia Iliaca Block, 30 ml Bupivacain %0,25
Ultrasound Guided Adductor Canal Block
Procedure/SurgeryUltrasound Guided Adductor Canal Block, 15ml Bupivacain %0,25
Ultrasound Guided iPACK Block
Procedure/SurgeryUltrasound Guided iPACK Block, 15ml Bupivacain %0,25
Treatment groups
Trial outcomes
Primary outcomes
Cumulative opioid consumption
Tramadol consumption will be recorded for 24 hours.
Secondary outcomes
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 to first postoperative analgesic requirement
The time to first postoperative analgesic requirement was recorded.
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.
Incidence of postoperative nausea and vomiting
Opioid side effects were recorded.
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