non objective disease
Conditions
Interventions
Use propofol or midazolam for sedation.
Control the sedation level in each participant based on the EEG monitoring and pharcokinetic and pharmacodynamic information.
Sponsors
Osaka University Graduate School of Medicine
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: Healthy male volunteers, without any disease and medications.
Exclusion criteria
Exclusion criteria: except for inclusion criteria
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluation of the scores for several memory tests in each sedation level. | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluation of several sensory perception and physiological responses in each sedation level. | — |
Countries
Japan
Contacts
Public ContactSatoshi Hagihira
Osaka University Graduate School of Medicine Department of Anesthesiology and Intensive Care Medicine
Outcome results
None listed