Comparison of Postoperative Outcomes Between Surgeries Anaesthetized With Propofol and Inhalational Anaesthetics

Sponsor
The University of Hong Kong (Other)
Overall Status
Unknown status
CT.gov ID
NCT03875872
Collaborator
(none)
6,000
1
6
1003.4

Study Details

Study Description

Brief Summary

Propofol used as anaesthesia in surgery had shown small postoperative analgesic benefits over inhalational anaesthetics in some meta-analyses. It was also associated with reduced risk of postoperative nausea and vomiting. Small sample of studies together with high heterogeneity prevented some meta-analyses to confirm propofol's effect for postoperative morphine consumption and other outcomes. Acute Pain Service data bank can provide an alternative way of evaluating postoperative outcomes of propofol anaesthetics through supplying a very large sample size in a more homogeneous setting. Retrospective study comparing propofol and inhalational anaesthetics on postoperative pain matched on patients' demographic and clinical data had been done for liver surgery. Propofol's benefits for postoperative pain and morphine consumption was confirmed but not for adverse effects.

This study plans to analyze the postoperative outcome data from an Acute Pain Service data bank in years 2015-17 to compare the anaesthetics of propofol and inhalational anaesthetics. Comprehensive regression adjustment for confounders are performed using all available patients' demographic, clinical and anaesthetic data. All major surgery types are included. Results will provide postoperative outcome differences between propofol and inhalational anaesthetics for all surgeries and for specific type of surgeries. The large sample bank will provide higher probability for detecting outcome difference between the anaesthetics for all the major surgical types.

Condition or Disease Intervention/Treatment Phase

Detailed Description

Objective: To compare the postoperative outcomes between surgeries anaesthetized with propofol and inhalational anaesthetics in the Acute Pain Service records of Queen Mary Hospital for years 2015-17

Methods:

Retrospective

Data collection

  1. Demographic data;

  2. Type of surgery;

  3. Type of anaesthetic techniques;

  4. Postoperative NRS pain scores (Rest and Moving) for Postop Days 1, 2 & 3;

  5. Accumulated amount of patient controlled analgesia (PCA) used in Postop Days 1, 2 & 3;

  6. Postoperative incidence of nausea, vomitting, dizziness and pruritus.

Study Design

Study Type:
Observational
Anticipated Enrollment :
6000 participants
Observational Model:
Other
Time Perspective:
Retrospective
Official Title:
Comparison of Postoperative Outcomes Between Surgeries Anaesthetized With Propofol and Inhalational Anaesthetics With Regression Controls for Confounders
Actual Study Start Date :
Feb 11, 2019
Anticipated Primary Completion Date :
Aug 12, 2019
Anticipated Study Completion Date :
Aug 12, 2019

Arms and Interventions

Arm Intervention/Treatment
Group propofol

Patients who had surgeries and were anaesthetized with propofol at Queen Mary Hospital, Hong Kong from Jan 2015 to Dec 2017

Drug: Propofol
Patients who had surgeries and were anaesthetized with propofol at Queen Mary Hospital, Hong Kong from Jan 2015 to Dec 2017

Group inhalation anaesthetics

Patients who had surgeries and were anaesthetized via inhalation at Queen Mary Hospital, Hong Kong from Jan 2015 to Dec 2017

Drug: inhalation anaesthetics
Patients who had surgeries and were anaesthetized via inhalation at Queen Mary Hospital, Hong Kong from Jan 2015 to Dec 2017

Outcome Measures

Primary Outcome Measures

  1. pain score [up to postoperative day 3]

    NRS (0-10) for both rest and moving

Secondary Outcome Measures

  1. analgesic consumption [up to postoperative day 3]

    amount of accumulated patient controlled analgesia (PCA) of morphine use

  2. Amount of patients with adverse events in post-operation [up to postoperative day 3]

    nausea and vomit, dizziness and pruritus

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  1. Postoperative outcomes from Acute Pain Service data bank between Jan 2015 and Dec 2017 in Queen Mary Hospital would be retrieved;

  2. Surgeries with general anaesthesia by either propofol or inhalational anaesthetics.

Exclusion Criteria:
  1. Essential data missed;

  2. Surgical types with small sample size below 30 for the data collection period.

Contacts and Locations

Locations

Site City State Country Postal Code
1 The University of Hong Kong Hong Kong Hong Kong

Sponsors and Collaborators

  • The University of Hong Kong

Investigators

  • Principal Investigator: Stanley SC Wong, MBBS, The University of Hong Kong

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Wong Sau Ching Stanley, Clinical Assistant Professor, The University of Hong Kong
ClinicalTrials.gov Identifier:
NCT03875872
Other Study ID Numbers:
  • UW19-182
First Posted:
Mar 15, 2019
Last Update Posted:
Mar 18, 2019
Last Verified:
Mar 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Wong Sau Ching Stanley, Clinical Assistant Professor, The University of Hong Kong
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 18, 2019