Clinical Trials Directory

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

TypeNameDescription
DRUGLidocaine 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
DRUGNormal salineIntravenous 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.