None listed
Conditions
Interventions
Drug : Prior to the conclusion of surgery, the treatment group will receive intravenous acetaminophen 1 g/100 mL administered over 15 minutes, while the control group will receive 0.9% normal saline 1
Sponsors
Konyang University Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Adults aged 19 to 65 years ASA physical status classification I or II Patients scheduled to undergo nasal surgery under general anesthesia Patients scheduled for endotracheal intubation Patients who have voluntarily provided written informed consent
Exclusion criteria
Exclusion criteria: Patients with contraindications to acetaminophen use (hepatic dysfunction, severe hepatic disease, etc.) Patients with obstructive sleep apnea Patients with cognitive impairment Patients undergoing emergency surgery Patients scheduled for postoperative transfer to the intensive care unit (ICU) Patients with alcohol or drug dependence Pregnant or breastfeeding women Patients who do not consent to study participation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of emergence agitation | — |
Secondary
| Measure | Time frame |
|---|---|
| Hemodynamic variables including heart rate and blood pressure;Time from discontinuation of anesthetic agent to extubation,;type and dose of analgesics administered in the post-anesthesia care unit;ncidence of postoperative nausea and vomiting (PONV) | — |
Countries
Korea, Republic of
Contacts
Public ContactKIM YOUSEOK
Konyang University Hospital
Outcome results
None listed