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Clinical Trial Summary

The goal of this prospective, interventionnal clinical trial is to assess if intravenous administration of linisol reduce the ED50 of propofol when administered using Target Controlled Infusion (TCI) during gastroscopy in healthy patients (ASA 1 and 2 patients). Prior to propofol sedation, participants will receive either an intravenous bolus of linisol (1.5 mg/kg) = treated group or placebo = control group.


Clinical Trial Description

n/a


Study Design


NCT number NCT06143410
Study type Interventional
Source Erasme University Hospital
Contact Céline Boudart, PhD
Phone +322555391+9
Email celine.boudart@hubruxelles.be
Status Recruiting
Phase N/A
Start date April 8, 2024
Completion date August 31, 2024