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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

TypeNameDescription
DEVICEEdmon (reg), BBraunexhaled 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.

Expiratory and Plasma Propofol Concentration in Gastrological Surgery Patients (NCT03817541) · Clinical Trials Directory