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UnknownNCT06143410

Intravenous Lidocaine to Reduce ED50 for Propofol Administered Using Target Controlled Infusion (TCI) During Gastroscopy

Does Intravenous Lidocaine Reduce ED 50 for Propofol Administered Using Target Controlled Infusion (TCI) During Gastroscopy in ASA 1 and 2 Patients.

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

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.

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 using target controlled infusion (TCI)
PROCEDUREgastroscopyesogastroduodenoscopy

Timeline

Start date
2024-04-08
Primary completion
2024-08-31
Completion
2024-08-31
First posted
2023-11-22
Last updated
2024-04-24

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT06143410. Inclusion in this directory is not an endorsement.