Study Stopped
The paper is about to publish on the same subject abroad, so the investigator decieded to stopped the study.
Comparison of Desflurane and Propofol on Quality of Recovery in Patients Undergoing Robotic or Laparoscopic Gastrectomy
1 other identifier
interventional
N/A
0 countries
N/A
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started Aug 2015
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 1, 2015
CompletedFirst Submitted
Initial submission to the registry
August 3, 2015
CompletedFirst Posted
Study publicly available on registry
August 5, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2015
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2015
CompletedFebruary 15, 2019
February 1, 2019
1 month
August 3, 2015
February 12, 2019
Conditions
Outcome Measures
Primary Outcomes (1)
Quality of recovery
The quality of recovery will be assessed with QoR-40 score.
Within 24 hours after the end of surgery
Study Arms (2)
Desflurane
ACTIVE COMPARATORAnesthesia is maintained with desflurane during surgery.
Propofol
EXPERIMENTALAnesthesia is maintained with propofol during surgery.
Interventions
Anesthesia is maintained with desflurane in Desflurane group according to the randomly allocated groups.
Eligibility Criteria
You may qualify if:
- adult patients aged over 20 yrs who are scheduled for laparoscopic or robotic gastrectomy, ASA 1 or 2.
You may not qualify if:
- patients with allergy to anesthetic agents
- body mass index more than 35 kg/m2
- pregnancy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 3, 2015
First Posted
August 5, 2015
Study Start
August 1, 2015
Primary Completion
September 1, 2015
Study Completion
September 1, 2015
Last Updated
February 15, 2019
Record last verified: 2019-02