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Expiratory and Plasma Propofol Concentration in Gastrological Surgery Patients

Bariatric Surgery Candidate Clinical Trial

Official title:
Expiratory and Plasma Propofol Concentration in Bariatric and Cholecystectomy Patients

Clinical Trial Summary

Determination of accuracy With Edmond (reg) expiratory propofol measurement Device, compared With concommitant plasma samples of propofol

Clinical Trial 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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03817541
Study type Interventional
Source Oslo University Hospital
Contact
Status Recruiting
Phase N/A
Start date November 14, 2018
Completion date December 31, 2020
View Details
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