None listed
Conditions
Interventions
Drug : 1 mg/kg of propofol for the control group (Group 1), propofol 1 mg/kg + ketamine 1/3 mg/kg for the experimental group 1 (Group2), and propofol 1mg/kg + ketamine 2/3mg/kg for the experimental gr
Sponsors
Chungnam National University Hospital
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: The research patients are selected from America society of anesthesiologist class 1 and 2 group women between 20 and 80 years of age.
Exclusion criteria
Exclusion criteria: Patients with America society of anesthesiologist class 3 or higher, patients younger than 20 years, patients older than 80 years, and patients who are contraindicated for use of the medication are excluded. BMI of 30 or more, who require the dosage of drug over the proper amount is excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Adduction motion during surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| blood pressure, heart rate, O2 saturation;consiousness level using by modified Ramsay sedation scale;incidence of apnea, and any intervention (jaw thrust, mask ventilation) | — |
Countries
Korea, Republic of
Contacts
Public Contactsookyoung youn
Chungnam National University Hospital
Outcome results
None listed