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
| Type | Name | Description |
|---|---|---|
| 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 |
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.