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Intravenous Lidocaine to Reduce Propofol Consumption During Gastroscopy.

NCT05944887 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 46

Last updated 2023-09-18

No results posted yet for this study

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

  • Diagnostic Gastroscopy

Interventions

DRUG

Lidocaine 2% Injectable Solution

administration of a bolus of lidocaine 1.5 mg/kg

DRUG

Saline administration as placebo

administration of a bolus of saline solution as a placebo

DRUG

Propofol injection

Sedation by total intravenous administration (TIVA) of propofol

PROCEDURE

gastroscopy

esogastroduodenoscopy

Sponsors & Collaborators

  • Erasme University Hospital

    lead OTHER

Principal Investigators

  • celine Boudart, MD PhD · Erasme University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-07-21
Primary Completion
2023-08-21
Completion
2023-08-25

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05944887 on ClinicalTrials.gov