Trials / Unknown
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
| 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 using target controlled infusion (TCI) |
| PROCEDURE | gastroscopy | esogastroduodenoscopy |
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.