None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Individuals who voluntarily provided written informed consent after receiving an explanation of the clinical trial 2) Male or female patients aged =20 years with colon or rectal cancer 3) Patients undergoing general anesthesia for laparoscopic colon or rectal resection 4) Patients classified as American Society of Anesthesiologists (ASA) physical status I–II 5) Patients scheduled to use patient-controlled analgesia (PCA) after surgery
Exclusion criteria
Exclusion criteria: 1) Patients with difficulty communicating 2) Patients with American Society of Anesthesiologists (ASA) physical status = III 3) Patients with prolonged QT interval on electrocardiography (>450 ms) 4) Patients with functional constipation (Bristol stool scale type 1 or 2) 5) Patients with irritable bowel syndrome 6) Patients with hypersensitivity to fentanyl, ketorolac, or 5-HT3 receptor antagonists 7) Patients receiving selective serotonin reuptake inhibitors (SSRIs) or serotonin–norepinephrine reuptake inhibitors (SNRIs) 8) Patients with a history of severe postoperative nausea and vomiting or severe motion sickness
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The elapsed time to first flatus after surgery;The elapsed time to first defecation after surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of postoperative nausea and vomiting;postoperative pain and analgesic consumption | — |
Countries
Korea, Republic of
Contacts
Jeonbuk National University Hospital