Clinical Trials Directory

Trials / Completed

CompletedNCT02784860

Effects of Intravenous Lidocaine During Sedation for Colonoscopy.

Investigation of the Effects of Intravenous Lidocaine Infusion During Sedation for Colonoscopy

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
40 (actual)
Sponsor
University of Liege · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Accepted

Summary

This study assesses the benefits of continuous intravenous lidocaine administration during sedation for colonoscopy. Sedation will consist of propofol infusion titrated to provide adequate working conditions to the gastroenterologist. Patients will be randomly allocated into two groups: lidocaine infusion (bolus of 1.5 mg/kg followed by a continuous infusion of 4 mg/kg/h) or the same volume of placebo (normal saline)

Detailed description

The potential benefits of lidocaine infusion will be tested on: * propofol consumption (primary outcome) * intraoperative respiratory depression * time for patient recovery * postoperative fatigue * postoperative pain * postoperative cognitive dysfunction

Conditions

Interventions

TypeNameDescription
DRUGLidocainePropofol (0.5 mg/kg or more) is titrated to provide loss of consciousness. Then in the lidocaine group, lidocaine 2% is administered as a bolus followed by a continuous intravenous infusion after loss of consciousness
DRUGnormal salinePropofol (0.5 mg/kg or more) is titrated to provide loss of consciousness. Then in the placebo group, the same volume of normal saline is administered after loss of consciousness

Timeline

Start date
2016-03-01
Primary completion
2016-09-01
Completion
2016-10-01
First posted
2016-05-27
Last updated
2018-01-03

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT02784860. Inclusion in this directory is not an endorsement.