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临床试验/NCT03875872
NCT03875872已完成不适用

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

The University of Hong Kong1 个研究点 分布在 1 个国家目标入组 3,922 人开始时间: 2019年2月11日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
3,922
试验地点
1
主要终点
pain score

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

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

研究组 & 干预措施

Group propofol

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

干预措施: Propofol (Drug)

Group inhalation anaesthetics

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

干预措施: inhalation anaesthetics (Drug)

结局指标

主要结局

pain score

时间窗: up to postoperative day 3

NRS (0-10) for both rest and moving

次要结局

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

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Wong Sau Ching Stanley

Clinical Assistant Professor

The University of Hong Kong

研究点 (1)

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