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

Sponsor
Yonsei University (Other)
Overall Status
Withdrawn
CT.gov ID
NCT02515968
Collaborator
(none)
0
Enrollment
2
Arms
1
Duration (Months)

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Study Start Date :
Aug 1, 2015
Anticipated Primary Completion Date :
Sep 1, 2015
Anticipated Study Completion Date :
Sep 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Desflurane

Anesthesia is maintained with desflurane during surgery.

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

Anesthesia is maintained with propofol during surgery.

Drug: Propofol
Other Names:
  • Anesthesia is maintained with propofol in Propofol group according to the randomly allocated groups.

    		•

    Outcome Measures

    Primary Outcome Measures

    1. Quality of recovery [Within 24 hours after the end of surgery]

      The quality of recovery will be assessed with QoR-40 score.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Yonsei University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Yonsei University
    ClinicalTrials.gov Identifier:
    NCT02515968
    Other Study ID Numbers:
    • 4-2015-0509
    First Posted:
    Aug 5, 2015
    Last Update Posted:
    Feb 15, 2019
    Last Verified:
    Feb 1, 2019
    Additional relevant MeSH terms:
    Propofol
    Desflurane

    Study Results

    No Results Posted as of Feb 15, 2019