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NCT02515968 Clinical Trial

Comparison of Desflurane and Propofol on Quality of Recovery in Patients Undergoing Robotic or Laparoscopic Gastrectomy

General Anesthesia Clinical Trial

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT02515968
Other study ID # 4-2015-0509
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date August 2015
Est. completion date September 2015

Study information
Verified date February 2019
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate whether propofol can improve quality of recovery compared to desflurane in patients undergoing robotic or laparoscopic gastrectomy.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date September 2015
Est. primary completion date September 2015
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria:

- adult patients aged over 20 yrs who are scheduled for laparoscopic or robotic gastrectomy, ASA 1 or 2.

Exclusion Criteria:

- patients with allergy to anesthetic agents

- body mass index more than 35 kg/m2

- pregnancy

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Desflurane
Anesthesia is maintained with desflurane in Desflurane group according to the randomly allocated groups.
• Propofol

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Yonsei University

Outcome
Type Measure Description Time frame Safety issue
Primary Quality of recovery The quality of recovery will be assessed with QoR-40 score. Within 24 hours after the end of surgery
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