Intra-op Lidocaine and Ketamine Effect on Postoperative Bowel Function
Colorectal Cancer
About this trial
This is an interventional prevention trial for Colorectal Cancer focused on measuring ketamine, lidocaine, postoperative ileus, randomized controlled trial, acute postoperative pain
Eligibility Criteria
Inclusion Criteria: age 18 to 79 booked for urgent or elective colon surgery undergoing a left, right, or transverse hemicolectomy via laparotomy Exclusion Criteria: patients requiring emergency surgery pregnant subjects or those who might be pregnant subjects allergic to lidocaine, ketamine, morphine, naproxen, or acetaminophen subjects with epidural analgesia subjects unable to understand and implement a Patient-Controlled Intravenous Analgesia system subjects who do not know English well enough to understand the consent form and assessments subjects with known hepatic or renal failure or cardiac dysrhythmias or atrioventricular block patients with pre-existing functional bowel motility disorders including Crohn's disease and ulcerative colitis daily use of laxatives, inability to have a bowel movement without laxatives, use of suppositories or enemas on a daily basis, or use of antimotility agents patients with Parkinson's disease
Sites / Locations
- Saskatoon Health Region, 410 22nd Street East