Comparison of Distal IPACK and Popliteal Plexus Block Combined With Femoral Triangle Block After Total Knee Arthroplasty
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: femoral triangle block and popliteal plexus block, Femoral triangle block and distal iPACK.
- Кому может быть актуально
- Состояния в реестре: Osteo Arthritis of the Knee. Базовые параметры: 18 лет — 85 лет · Все.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- Turkey (Türkiye)
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Обзор
This study aims to investigate the effect of femoral triangle block combined with popliteal plexus block and distal IPACK block on postoperative pain after total knee arthroplasty (TKA)
Подробное описание
Popliteal Plexus Block (PPB) is a new nerve block technique that has been shown to anaesthetise nerves involved in the innervation of the posterior part of the knee joint.
The IPACK (interspace between the popliteal artery and capsule of the posterior knee) block is a regional anesthesia technique in which a local anesthetic is infiltrated under ultrasound guidance between the popliteal artery and the capsule of the posterior knee. This technique blocks the branches of the obturator nerve, the common peroneal nerve, and the tibial nerve in the popliteal region. In the context of knee arthroplasty, the application of the IPACK block has been associated with lower scores for ambulatory pain, lower scores for resting pain, and reduced morphine consumption.
Although both techniques of blockade seem to be efficient in the context of analgesia for the posterior part of the knee after TKA. No study compares these two blocks as part of multimodal analgesia to provide pain relief after TKA.
This study aimed to evaluate the analgesic effect of PPB or distal IPACK, in addition to femoral triangle block, as a component of a multimodal analgesic regimen after TKA.
Вмешательства
- Устройство femoral triangle block and popliteal plexus block
Single dose bolus, 10 ml 5% bupivacaine will be used for FTB, 10 ml 5% bupivacaine will be used for PPB - Устройство Femoral triangle block and distal iPACK
Single dose bolus, 10 ml 5% bupivacaine will be used for FTB, 10 ml 5% bupivacaine will be used for distal iPACK
Первичные конечные точки
- Opioid consumption [Срок оценки: 24 hours]
Вторичные конечные точки (11)
- NRS scores [Срок оценки: 48 hours]
- Range of knee motion [Срок оценки: 48 hours]
- Patient mobilization [Срок оценки: 48 hours]
- Post-block Maximum Voluntary Isometric Contraction (MVIC) by knee extension, calculated as a percentage of the Pre-block baseline value [Срок оценки: A 60-minute interval is between pre-block and post-block MVIC assessments]
- Post-block MVIC by ankle plantarflexion, calculated as a percentage of the Pre-block baseline value [Срок оценки: A 60-minute interval is between pre-block and post-block MVIC assessments]
- Post-block MVIC by ankle dorsiflexion, calculated as a percentage of the Pre-block baseline value [Срок оценки: A 60 minutes interval is between pre-block and post-block MVIC assessments]
- Muscle strength of knee extension, graded by Manual Muscle Test (MMT) [Срок оценки: Assessed pre-block, post-block (60 minutes after pre-block), and postoperative 5 hours]
- Muscle strength of ankle plantarflexion, graded by MMT [Срок оценки: Assessed pre-block, post-block (60 minutes after pre-block) and postoperative 5 hours]
- Muscle strength of ankle dorsiflexion, graded by MMT [Срок оценки: Assessed pre-block, post-block (60 minutes after pre-block) and postoperative 5 hours]
- Incidence of rebound pain [Срок оценки: Postoperative 24 hours]
- Quality of Recovery 15 Score [Срок оценки: Postoperative Day 1]
Критерии участия
Критерии включения
- Patients undergoing total knee arthroplasty under spinal anesthesia
- American Society of Anesthesiologists (ASA) status I-III
- Patients who give informed consent
Критерии исключения
- Patients unable to cooperate
- Kidney disease with GFR < 50 ml/min
- Daily opioid consumption > 1 month
- Allergy to local anesthetics
- Neurological problems of the lower extremity
- Contraindications to peripheral nerve blocks
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Параллельные группы
- Маскирование
- Четверное слепое
- Основная цель
- Лечение
Центры проведения
Turkey (Türkiye) · 1 центр
- Karaman Training and Research Hospital, Karaman, Karaman 70200 — Karaman
Идентификаторы
NCT: NCT07130552 · 06-2022/16