Patients indicated for elective open gastrectomy were screened, enrolled, and randomised between October 2021 and September 2023. The patients were randomised to either Group A (intervention-continuous bupivacaine) or Group B (control-NaCl saline). The primary outcome measures were the quantity of an opioid analgesic administered during the initial 72 h post-surgery and the level of postoperative pain as indicated by the visual analogue scale (VAS
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Enrollment
60
The surgical procedure involved an upper middle laparotomy. Prior to the surgery, standard preoperative monitoring was conducted, including venous access placement, pulse oximetry, electrocardiography, and automated non-invasive arterial blood pressure measurement. General anesthesia was administered through both intravenous and endotracheal methods following standard protocols.
Riga East Clinical University Hospital
Riga, Riga, Latvia
Postoperative Pain Assessment
VAS
Time frame: 12 weeks
Postoperative Recovery
Postoperative bowel movement
Time frame: 12 weeks
Rescue Pain Management and Analgesia
Use of additional NSAIDs
Time frame: 12 weeks
Postoperative recovery
Postoperative days
Time frame: 12 weeks
Opioids
Use of opioids postoperatively
Time frame: 12 weeks
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