Pain Clinical Trial
Official title:
Efficacy of the Ultrasound-guidedTransversus Abdominis Plane (TAP) Block on Postoperative Pain Control in Open Aortic Abdominal Aneurysm Repair Surgery
The ETAP study aim to assess the effect of the addition of an ultrasound-guided transversus abdominis plane (TAP) block to a multimodal intravenous analgesia protocol on the postoperative pain control in open surgical repair of abdominal aortic aneurysm. The ETAP study is a single-center open-label randomized controlled trial. Half of patients included will receive the association of TAP block and multimodal intravenous analgesia, and the other half will receive the multimodal intravenous analgesia alone. The multimodal intravenous analgesia includes intravenous paracetamol and intravenous patient-controlled analgesia with morphine.
The open repair of abdominal aortic aneurysm (AAA) is a painful surgery. Patients suffering
from AAA are at high risk of perioperative cardiovascular and pulmonary complications. It
has been previously suggested that a bad perioperative pain control could increase the
incidence of such complications.
Intravenous patient-controlled analgesia (PCA) with morphine is widely considered as the
gold standard treatment of the postoperative pain in open repair of AAA. High dose of
morphine are often required and could delay the postoperative recovery and discharge. Side
effects of morphine, such as respiratory depression, nausea, vomiting or pruritus, are
responsible for patient discomfort and dissatisfaction when high doses are used.
The efficacy of the ultrasound-guided transversus abdominis plane (TAP) block has been
described for pain management following abdominal surgery, such as gastrectomy or kidney
transplantation. The efficacy of the association of TAP block and PCA with morphine was
higher than multimodal intravenous analgesia including PCA with morphine and than the
combination of PCA with morphine and epidural analgesia. To our knowledge, the efficacy of
the ultrasound-guided TAP block has never been studied for the postoperative pain control in
AAA surgery.
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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