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
| Type | Name | Description |
|---|---|---|
| DRUG | Lidocaine | Propofol (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 |
| DRUG | normal saline | Propofol (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.