Study to Investigate TIVA With Propofol on Postoperative Pain and Side Effects

Withdrawn

• Conditions: Postoperative Pain
• Interventions: Procedure: general anaesthesia; Drug: Propofol

• Registration Number: NCT03058354
• Lead Sponsor: The University of Hong Kong

Brief Summary

Propofol is a commonly used anaesthetic with rapid recovery and less side effects and total intravenous anaesthesia (TIVA) with propofol is a common technique now. The reduction on certain serum pro- inflammatory cytokines may lead to more smooth post- surgical recovery.

Recent case report proved the analgesic effect of propofol infusion. However other animal and clinical studies showed controversial result.

The aim of this retrospective study is to investigate the postoperative analgesic effects and side effects of intraoperative TIVA with propofol in patient undergoing surgery at Queen Mary Hospital, Hong Kong between 2014 to 2016.

Detailed Description

Objectives:

1. To investigate the analgesic effects of propofol.

2. To evaluate the effect of propofol on postoperative adverse events.

Methods:

Retrospective audit.

Data Collection:

1. Demographic data;

2. Types of analgesic techniques;

3. Type of pain relief modalities;

4. Pain score up to 72 hours postoperatively;

5. Postoperative opioid consumption;

6. Incidence of adverse events during APS care;

7. Patients' satisfaction on pain relief.

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study Start: 2017-01-01
• Study First Submitted: 2017-02-07
• Study First Submitted QC: 2017-02-17
• Study First Posted: 2017-02-20
• Primary Completion: 2019-12-31
• Study Completion: 2020-12-31
• Status Verified: 2022-10
• Last Update Submitted: 2022-10-11
• Last Update Posted: 2022-10-13

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

• Anaesthetic records and acute pain service records of patient undergone surgery between 2014 to 2016 in Queen Mary Hospital would be retrieved from the computer.

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Exclusion Criteria

• Essential data were missing.
• Patient participating in other research projects.
• Changes in postoperative pain management technique.
• Patients could not be assessed post-operatively for pain (i.e. post-operative IPPV)

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Group GA	general anaesthesia	Patient undergoing surgery at Queen Mary Hospital, Hong Kong between 2014 to 2016 using general anaesthesia methods other than intraoperative TIVA with propofol.
Group TIVA	Propofol	Patient undergoing surgery at Queen Mary Hospital, Hong Kong between 2014 to 2016 using intraoperative TIVA with propofol.

Primary Outcome Measures

Name	Time	Method
pain score	up to postoperative day 3	pain score using numeral rating scale

Secondary Outcome Measures

Name	Time	Method
analgesic consumption	up to postoperative day 3	analgesic consumption base on patient drug record

Trial Locations

Locations (1)

The University of Hong Kong; 🇭🇰 Hong Kong, Hong Kong