Trials / Completed
CompletedNCT02543411
Use of Lidocaine in Endoscopic Submucosal Dissection
Effect of Intravenous Lidocaine During Endoscopic Submucosal Dissection for Gastric Neoplasm
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 66 (actual)
- Sponsor
- Severance Hospital · Academic / Other
- Sex
- All
- Age
- 20 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
The primary purpose of this study is to investigate the effects of lidocaine on the total administered dose of fentanyl during sedation for endoscopic mucosal resection. The secondary purpose of this study is to investigate the effects of lidocaine on pain score related with endoscopic mucosal resection at time of 30 min, 6 hr, and 24 hr after procedure.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Lidocaine 1% | Intravenous administration as bolus of lidocaine 1.5 mg/kg before sedation and infusion of lidocaine 2 mg/kg/hr during sedation. Sedation with fentanyl and propofol |
| DRUG | Normal saline | Intravenous administration as bolus of normal saline 0.15 mL/kg before sedation and infusion of normal saline 0.2 mL/kg/hr during sedation. Sedation with fentanyl and propofol |
Timeline
- Start date
- 2015-09-01
- Primary completion
- 2015-11-01
- First posted
- 2015-09-07
- Last updated
- 2015-12-15
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT02543411. Inclusion in this directory is not an endorsement.