colonic or rectal disease requiring surgery (patients undergoing laparoscopic colectomy or proctectomy)
Conditions
Interventions
Propofol group: administration of propofol (5-6 mg/kg/hr) for sedative
Sevoflurane group: administration of sevoflurane (1-1.5%) for sedative
Sponsors
Bellland General Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: patients undergoing laparoscopic colectomy or proctectomy
Exclusion criteria
Exclusion criteria: patients with glaucoma, obstractive pulmonary disease (FEV1%<50), without informed concent, past history of jaundice or high fever with volatile anesthetics, pregnant woman, past history of abnormal reaction to sevoflurane or propofol, patients recongnised as inadequate for this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| intraocular pressure 1)before induction of general anesthesia 2)just after induction of general anesthesia 3)just after pneumoperitoneum achievement 4)just after position changing to Trendelenburg (head lower) position 5)just after changing to flat position 6)just after terminating pneumoperitoneum 7)just after extubation | — |
Secondary
| Measure | Time frame |
|---|---|
| blood pressure, heart rate, body temperature, airway pressure, endtidal carbon dioxide, tilt angle of the bed, partial carbon dioxide pressure in arterial blood, operative time, anesthetic time, total fluid infusion, total operative bleeding, total volume of urine, total transfusion, total dose of fentanyl, total dose of remifentanil, visual dysfunction after surgery | — |
Countries
Japan
Contacts
Public ContactYasumitsu Nomura
Bellland General Hospital Department of Anesthesia
Outcome results
None listed