Riga East Clinical University Hospital
Riga, 1039, Latvia
NCT Number: NCT07634731
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
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Riga, 1039, Latvia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
Time frame: 12 weeks
VAS
Time frame: 12 weeks
Postoperative bowel movement
Time frame: 12 weeks
Use of additional NSAIDs
Time frame: 12 weeks
Postoperative days
Time frame: 12 weeks
Use of opioids postoperatively
Igors Ivanovs
Other Gov
Comparison of Bilateral Rectus Sheath Block and Thoracic Epidural Analgesia for Postoperative Pain Control After Open Gastrectomy
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