Patients who will have elective gynecologic surgery
Conditions
Interventions
An administration of Acetaminophen dose: 15 mg/kg (max 1000 mg) duration of administration: 15 minutes timing: Primary dosage is performed just after an anesthetic induction. Secondary dosage is
Sponsors
University of the Ryukyus
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Patients who will have elective, gynecologic abdominal surgery Predicted surgical time is over 2 hour Patients' physical status(ASA) are 1 or 2 Patients without an impaired liver function Patients without disturbance of consciousness
Exclusion criteria
Exclusion criteria: Insufficient record and measurement Patients who refuse to participate this study Patient with suspicion of allergy of Acetaminophen Patient with acute toxicity of Lidocaine or Ropivacaine Patient require critical care and mechanical ventilation in ICU after surgery Patient who is determined to be excluded from the study due to any reason by the study doctor
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The incidence of postoperative shivering | — |
Secondary
| Measure | Time frame |
|---|---|
| The score of postoperative shivering The change of intraoperative and postoperative core temperature The incidence of postoperative nausea and vomitting The values of pain intensity measured on visual analog scales | — |
Countries
Japan
Contacts
Public ContactTakahiro Tadokoro
University of the Ryukyus Department of Anesthesiology, Faculty of Medicine
Outcome results
None listed