Overview

A Comparison of Efficacy and Safety During Endoscopic Submucosal Dissection Between Dexmedetomidine-remifentanil and Propofol-remifentanil

Status:
Completed
Trial end date:
2013-03-01
Target enrollment:
0
Participant gender:
All
Summary
Adequate, safe sedation is essential for Endoscopic submucosal dissection. Dexmedetomidine is a potent and selective a2-adrenoceptor agonist used for sedative and analgesic effects, but it is limited to use alone. The investigators designed this study to compare the effect and safety of two sedatives, dexmedetomidine and propofol in Endoscopic Submucosal Dissection (ESD), when sufficient analgesia-remifentanil is administered all throughout the procedure.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Yonsei University
Treatments:
Dexmedetomidine
Propofol
Remifentanil
Criteria
Inclusion Criteria:

- Age ≥20

- American Society of Anaesthesiologists(ASA) physical status classification I~III

- Early gastric cancer patients who were scheduled for Endoscopic submucosal dissection

Exclusion Criteria:

- Age < 20

- American Society of Anaesthesiologists(ASA) physical status classification IV

- those with end-organ diseases (i.e. heart failure, respiratory failure, hepatic
failure, renal failure)

- known drug allergies or history of drug abuse

- psychological disease