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The aim of this study is to validate that an effect compartment concentration for loss of consciousness (LOC) was varied according to different Keo value.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Diprifusor group | Active Comparator | Propofol was infused via Diprifusor TCI (Target-controlled infusion) |
|
| Orchestra group | Experimental | Propofol was infused via Orchestra TCI |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Diprifusor (Target-controlled infusion) | Device | Two TCI devices with different Teo and same Marsh PK model |
|
| Measure | Description | Time Frame |
|---|---|---|
| Estimated effect-site propofol concentration at loss of consciousness | after propofol infusion |
| Measure | Description | Time Frame |
|---|---|---|
| Time to loss of consciousness | after propofol infusion |
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Inclusion Criteria:
Exclusion Criteria:
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| Orchestra (Target-controlled infusion) | Device | Two TCI devices with different Teo and same Marsh PK model |
|
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