Pain, Postoperative Clinical Trial
Official title:
Laparoscopic-guided Transversus Abdominis Plane (TAP) Block for Postoperative Pain Control in Patients Undergoing Laparoscopic Roux-en-Y Gastric Bypass
A prospective randomized trial will be performed. Patients undergoing gastric bypass will be
randomized into 2 groups: patients undergoing laparoscopic-guided transversus abdominis
plane (TAP) block as part of multimodal analgesia (Group 1), associated with postoperative
intravenous analgesia, and patients receiving only postoperative intravenous analgesia
(Group 2).
Postoperative pain will be assessed with a Visual Analogic Scale 24h after surgery and
morphine needs will be quantified.
A prospective randomized trial will be performed. Patients undergoing laparoscopic Roux-en-Y
gastric bypass will be randomized into 2 groups: patients undergoing laparoscopic-guided TAP
block with 30 ml Bupivacaine 0.5%, as part of multimodal analgesia (Group 1), associated
with postoperative intravenous analgesia (Metamizol 2g/8h and Acetaminophen 1g/8h), and
patients receiving only postoperative intravenous analgesia (Metamizol 2g/8h and
Acetaminophen 1g/8h) (Group 2).
Postoperative pain will be assessed with a Visual Analogic Scale 24 hours after surgery and
morphine needs will be quantified.
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