Study to Investigate TIVA With Propofol on Postoperative Pain and Side Effects
NCT ID: NCT03058354
Last Updated: 2022-10-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
OBSERVATIONAL
2017-01-01
2020-12-31
Brief Summary
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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.
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Detailed Description
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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.
Conditions
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Study Design
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OTHER
RETROSPECTIVE
Study Groups
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Group TIVA
Patient undergoing surgery at Queen Mary Hospital, Hong Kong between 2014 to 2016 using intraoperative TIVA with propofol.
Propofol
Patient undergoing surgery at Queen Mary Hospital, Hong Kong between 2014 to 2016 using intraoperative TIVA with propofol.
Group GA
Patient undergoing surgery at Queen Mary Hospital, Hong Kong between 2014 to 2016 using general anaesthesia methods other than intraoperative TIVA with propofol.
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.
Interventions
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Propofol
Patient undergoing surgery at Queen Mary Hospital, Hong Kong between 2014 to 2016 using intraoperative TIVA with propofol.
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.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* 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)
ALL
No
Sponsors
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The University of Hong Kong
OTHER
Responsible Party
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Wong Sau Ching Stanley
Clinical Assistant Professor
Principal Investigators
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Stanley SC Wong, MBBS
Role: PRINCIPAL_INVESTIGATOR
The University of Hong Kong
Locations
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The University of Hong Kong
Hong Kong, , Hong Kong
Countries
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Other Identifiers
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UW17-001
Identifier Type: -
Identifier Source: org_study_id
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