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Clinical Trials/NCT03875872
NCT03875872
Completed
Not Applicable

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

The University of Hong Kong1 site in 1 country3,922 target enrollmentFebruary 11, 2019

Overview

Phase
Not Applicable
Intervention
Propofol
Conditions
Acute Pain
Sponsor
The University of Hong Kong
Enrollment
3922
Locations
1
Primary Endpoint
pain score
Status
Completed
Last Updated
2 years ago

Overview

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.

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.

Registry
clinicaltrials.gov
Start Date
February 11, 2019
End Date
August 12, 2019
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Wong Sau Ching Stanley

Clinical Assistant Professor

The University of Hong Kong

Eligibility Criteria

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.

Arms & Interventions

Group propofol

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

Intervention: Propofol

Group inhalation anaesthetics

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

Intervention: inhalation anaesthetics

Outcomes

Primary Outcomes

pain score

Time Frame: up to postoperative day 3

NRS (0-10) for both rest and moving

Secondary Outcomes

  • analgesic consumption(up to postoperative day 3)
  • Amount of patients with adverse events in post-operation(up to postoperative day 3)

Study Sites (1)

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