Dental patients undergoing total intravenous anesthesia
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)BMI is less than 30, 2)ASA is PS 1 or 2, 3)Anesthesia time will be less than 5 hours, 4)Patients undergoing dental treatment or minor oral surgery, 5)No need receiving opioid analgesics for postoperative analgesia
Exclusion criteria
Exclusion criteria: 1)Patients with contraindications for propofol, remifentanil, rocuronium, 2)Patients who are judged to be inappropriate for study participation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1)Blood concentration of propofol at the discontinuation of propofol and tracheal extubation, 2)Time from the discontinuation of propofol to tracheal extubation and 3)BIS value at tracheal extubation | — |
Secondary
| Measure | Time frame |
|---|---|
| 1)Propofol amount and average infusion rate of propofol, 2)Estimated blood concentration of propofol at the discontinuation of propofol and tracheal extubation, 3)Remifentanil amount and average infusion rate of remifentanil, 4)BIS values before & during anesthesia, and at the discontinuation of propofol. | — |
Countries
Japan
Contacts
Okayama University Hospital Department of Dental Anesthesiology