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NCT Number: NCT03875872

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

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

The University of Hong Kong

Hong Kong

About this study

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

  • Demographic data;
  • Type of surgery;
  • Type of anaesthetic techniques;
  • Postoperative NRS pain scores (Rest and Moving) for Postop Days 1, 2 & 3;
  • Accumulated amount of patient controlled analgesia (PCA) used in Postop Days 1, 2 & 3;
  • Postoperative incidence of nausea, vomitting, dizziness and pruritus.

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Postoperative outcomes from Acute Pain Service data bank between Jan 2015 and Dec 2017 in Queen Mary Hospital would be retrieved;
  • Surgeries with general anaesthesia by either propofol or inhalational anaesthetics.

Exclusion criteria

  • Essential data missed;
  • Surgical types with small sample size below 30 for the data collection period.

Treatment and study plan

Propofol

Drug

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

inhalation anaesthetics

Drug

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

Primary outcomes

  1. pain score

    Time frame: up to postoperative day 3

    NRS (0-10) for both rest and moving

Secondary outcomes

  1. analgesic consumption

    Time frame: 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

    Time frame: up to postoperative day 3

    nausea and vomit, dizziness and pruritus

Sponsors and collaborators

Lead sponsor

The University of Hong Kong

Other

Registry information

Official study title

Comparison of Postoperative Outcomes Between Surgeries Anaesthetized With Propofol and Inhalational Anaesthetics With Regression Controls for Confounders

Important dates

Study start
2019
Primary completion
2019
Study completion
2019
First posted
Mar 15, 2019
Registry last updated
May 10, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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