Clinical Trials Directory

Trials / Completed

CompletedNCT05407870

Efficacy and Safety of Etomidate Sedation in Gastric Endoscopic Submucosal Dissection

A Comparative Study of the Efficacy and Safety of Etomidate Compared to Propofol in Gastric Endoscopic Submucosal Dissection: a Prospective, Single-center, Randomized, Double-blind, Non-inferiority Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
138 (actual)
Sponsor
Korea University Anam Hospital · Academic / Other
Sex
All
Age
19 Years – 80 Years
Healthy volunteers
Not accepted

Summary

During endoscopy, the patient is sedated to relieve pain and improve the ease of the procedure. Sedation endoscopy using propofol is effective, but has the disadvantage that cardiopulmonary side effects are frequently observed. However, etomidate is known to have hemodynamic and respiratory stability.The purpose of this study was to compare the efficacy and safety of etomidate and propofol in sedated gastric endoscopic submucosal dissection.

Conditions

Interventions

TypeNameDescription
DRUGEtomidate InjectionProofol and etomidate are drugs used for sedation and have the same white color. Gastric endoscopic submucosal dissection is performed using propofol in the control group and etomidate in the experimental group. Efficacy and safety of sedatives were confirmed using propofol and etomidate.
DRUGPropofol InjectionProofol and etomidate are drugs used for sedation and have the same white color. Gastric endoscopic submucosal dissection is performed using propofol in the control group and etomidate in the experimental group. Efficacy and safety of sedatives were confirmed using propofol and etomidate.

Timeline

Start date
2022-06-09
Primary completion
2022-11-24
Completion
2022-11-24
First posted
2022-06-07
Last updated
2024-11-12

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT05407870. Inclusion in this directory is not an endorsement.