Trials / Completed
CompletedNCT01091350
Influence of Equilibration Rate Constant (ke0) of Propofol on the Effect Site Concentration for Loss of Consciousness
Influence of Equilibration Rate Constant (ke0) of Propofol on the Effect-site Concentration for Loss of Consciousness
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (actual)
- Sponsor
- Seoul National University Hospital · Academic / Other
- Sex
- Female
- Age
- 20 Years – 60 Years
- Healthy volunteers
- Not accepted
Summary
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Diprifusor (Target-controlled infusion) | Two TCI devices with different Teo and same Marsh PK model |
| DEVICE | Orchestra (Target-controlled infusion) | Two TCI devices with different Teo and same Marsh PK model |
Timeline
- Start date
- 2009-05-01
- Primary completion
- 2009-10-01
- Completion
- 2009-11-01
- First posted
- 2010-03-24
- Last updated
- 2013-05-31
Source: ClinicalTrials.gov record NCT01091350. Inclusion in this directory is not an endorsement.