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Clinical Trials/NCT05930184
NCT05930184
Recruiting
Phase 2

Comparison of Laparoscopic Guided Peri-wound Transversus Abdominis Plane Block With Bupivacaine Versus Local Wound Infiltration on Post-op Opioid Use in Laparoscopic Sleeve Gastrectomy, A Prospective Randomized Controlled Study

Khon Kaen University1 site in 1 country98 target enrollmentApril 29, 2023
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ConditionsMorbid ObesityLaparoscopic Sleeve GastrectomyTransversus Abdominis Plane BlockLocal Wound InfiltrationBupivacineOpioid Use

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Morbid Obesity
Sponsor
Khon Kaen University
Enrollment
98
Locations
1
Primary Endpoint
Cumulative morphine use
Status
Recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The goal of this randomized controlled trial is to compare laparoscopic guided peri-wound Transversus Abdominis Plane Block and bupivacaine versus local wound infiltration effect on reducing post-op opioid use in Laparoscopic Sleeve gastrectomy. The main questions it aims to answer are:

• Can laparoscopic guided peri-wound Transversus Abdominis Plane Block reduced post operative morphine usage when comparing with local wound port site infiltration.

Participants will be randomize into 2 group

  • peri-wound Transversus Abdominis Plane Block
  • local wound port site infiltration
Registry
clinicaltrials.gov
Start Date
April 29, 2023
End Date
December 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Thanatat panitphong

Primary investigator

Khon Kaen University

Eligibility Criteria

Inclusion Criteria

  • •patient undergoing LSG at Sringarind hospital as indicated by Thai guideline

Exclusion Criteria

  • •Allergic/contraindicated to bupivacaine, morphine, fentanyl, NSAIDs or Nefopam
  • •Unable to describe pain score Opioid addict
  • •denied consent

Outcomes

Primary Outcomes

Cumulative morphine use

Time Frame: 48hours after intervention

Secondary Outcomes

  • opioid side effect(within admission)
  • length of hospital stay(within admission)
  • PACU time(1day after intervention)
  • postop complication(2weeks after intervention)
  • Post op VAS pain score(48hours after intervention)

Study Sites (1)

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