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The goal of this clinical trial is to assess if intravenous administration of linisol reduce the propofol consumption and the sides effects of sedation 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.
After the gastroscopy, patients will be asked to complete a satisfaction questionnaire
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46 participants in 2 patient groups, including a placebo group
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Omar Assam, MD; celine boudart, MD PhD
Data sourced from clinicaltrials.gov
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