Clinical Trials Directory

Trials / Completed

CompletedNCT05944887

Intravenous Lidocaine to Reduce Propofol Consumption During Gastroscopy.

Does Intravenous Lidocaine Reduce Propofol Consumption and the Side Effects of Sedation During Gastroscopy in ASA 1 and 2 Patients.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
46 (actual)
Sponsor
Erasme University Hospital · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

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

Conditions

Interventions

TypeNameDescription
DRUGLidocaine 2% Injectable Solutionadministration of a bolus of lidocaine 1.5 mg/kg
DRUGSaline administration as placeboadministration of a bolus of saline solution as a placebo
DRUGPropofol injectionSedation by total intravenous administration (TIVA) of propofol
PROCEDUREgastroscopyesogastroduodenoscopy

Timeline

Start date
2023-07-21
Primary completion
2023-08-21
Completion
2023-08-25
First posted
2023-07-13
Last updated
2023-09-18

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT05944887. Inclusion in this directory is not an endorsement.