Trials / Unknown
UnknownNCT03817541
Expiratory and Plasma Propofol Concentration in Gastrological Surgery Patients
Expiratory and Plasma Propofol Concentration in Bariatric and Cholecystectomy Patients
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 30 (estimated)
- Sponsor
- Oslo University Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 60 Years
- Healthy volunteers
- Not accepted
Summary
Determination of accuracy With Edmond (reg) expiratory propofol measurement Device, compared With concommitant plasma samples of propofol
Detailed description
Edmon (trade mark) is a New Device from BBraun, measuring the expiratory concentration of propofol in anaesthetized patients. The investigators will test the accuracy and stability of such measurements in comparison With plasma propofol Levels. The investigators will test during target Control infusion (Marsh model) and assumed stable plasma Levels. Plasma samples of propofol will be taken for comparison With exhaled propofol.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Edmon (reg), BBraun | exhaled propofol will be compared With plasma propofol values |
Timeline
- Start date
- 2018-11-14
- Primary completion
- 2019-06-30
- Completion
- 2020-12-31
- First posted
- 2019-01-25
- Last updated
- 2019-02-05
Locations
1 site across 1 country: Norway
Source: ClinicalTrials.gov record NCT03817541. Inclusion in this directory is not an endorsement.