None listed
Conditions
Interventions
Drug : 30 minutes before the expected end of the surgery, the maxigesic group receives 1 vial (100 mL) of the maxigesic formula, and the control group receives 100 mL of normal saline over 15 minutes.
Sponsors
Konyang University Hospital
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. Female patients aged 19 to 64 who require endotracheal intubation during gynecological surgery 2. According to the American Society of Anesthesiologist's physical status classification, 1 to 3 patients.
Exclusion criteria
Exclusion criteria: - Patients with sore throat, cough, and hoarseness before surgery - Patients with symptoms of upper respiratory tract infection before surgery - Patients who are expected difficult intubation - Psychiatric patients - Patients with cognitive impairment - Contraindicated use of acetaminophen or ibuprofen (e.g., history of hypersensitivity reactions, gastrointestinal ulcers, severe renal impairment) - When the surgical method is changed from laparoscopic to laparotomy during surgery - Patients with active alcoholism - Patients with severe blood abnormalities, severe liver disorders, severe kidney disorders, severe heart failure, and severe hypertension - Patients with asthma or a history - Patients with pain before and after coronary artery bypass surgery - If you are taking concomitant medications (eg, barbiturates, tricyclic antidepressants, high-dose methotrexate) - In other cases where the researcher is considered inappropriate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| postoperative sore throat | — |
Secondary
| Measure | Time frame |
|---|---|
| time to extubation, emergence agitation, pain grade, requirement of analgesic, postoperative sore throat at the ward. | — |
Countries
Korea, Republic of
Contacts
Public ContactSung-Ae Cho
Konyang University Hospital
Outcome results
None listed