Intraoperative TIVA With Propofol on Postoperative Pain and Side Effects After Liver Resection Surgery
Retrospective Study to Investigate Intraoperative TIVA With Propofol on Postoperative Pain and Side Effects After Liver Resection Surgery
1 other identifier
observational
95
1 country
1
Brief Summary
Postoperative pain can be severe after liver resection surgery. However, postoperative pain management may be difficult for this group of patients. Opioidergic neurotransmission may be altered in cirrhotic patients and selectively increasing receptor affinity for opioids. Large dose of strong opioid may be required to achieve adequate pain control. However, this may not be possible due to the side effect of opioid and liver dysfunction after liver resection. Propofol is a commonly used anaesthetic with rapid recovery and less side effects and TIVA (total intravenous analgesia) 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 liver resection surgery at Queen Mary Hospital, Hong Kong between 2010 to 2012.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Aug 2014
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 27, 2014
CompletedFirst Posted
Study publicly available on registry
July 1, 2014
CompletedStudy Start
First participant enrolled
August 1, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 22, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
February 22, 2016
CompletedMay 16, 2024
May 1, 2024
1.6 years
June 27, 2014
May 14, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Postoperative pain score
From postoperative 1 hour to postoperative 72 hour
Secondary Outcomes (1)
Adverse event
From postoperative 1 hour to postoperative 72 hour
Other Outcomes (1)
Analgesic consumption
From postoperative 1 hour to postoperative 72 hour
Eligibility Criteria
Patient undergone liver resection surgery between 2010 to 2012 in Queen Mary Hospital
You may qualify if:
- Patient undergone liver resection surgery between 2010 to 2012 in Queen Mary Hospital
You may not qualify if:
- 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)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of Anaesthesiology, The University of Hong Kong
Hong Kong, Hong Kong, China
Related Publications (1)
Chan AC, Qiu Q, Choi SW, Wong SS, Chan AC, Irwin MG, Cheung CW. Effects of Intra-Operative Total Intravenous Anaesthesia with Propofol versus Inhalational Anaesthesia with Sevoflurane on Post-Operative Pain in Liver Surgery: A Retrospective Case-Control Study. PLoS One. 2016 Feb 22;11(2):e0149753. doi: 10.1371/journal.pone.0149753. eCollection 2016.
PMID: 26901037DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Chi Wai Cheung, MD
Department of Anaesthesiology, The University of Hong Kong
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Clinical Associate Professor
Study Record Dates
First Submitted
June 27, 2014
First Posted
July 1, 2014
Study Start
August 1, 2014
Primary Completion
February 22, 2016
Study Completion
February 22, 2016
Last Updated
May 16, 2024
Record last verified: 2024-05