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Clinical Trials/NCT06265402
NCT06265402
Recruiting
Not Applicable

Comparison Between US Guided Retrolaminar Block and Transversus Abdominis Plane Block for Post Operative Analgesia in Patient Undergoing Abdominal Plastic Surgery

Tanta University1 site in 1 country90 target enrollmentJanuary 15, 2024
ConditionsBlock

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Block
Sponsor
Tanta University
Enrollment
90
Locations
1
Primary Endpoint
Total dose of morphine consumption in the first postoperative 24hours
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The aim of the study is to compare the analgesic efficacy of Us guided retrolaminar block versus transversus abdominis plane block in patient under going abdominal plastic surgery

Detailed Description

Pain from intra abdominal surgery is a combination of somatic and visceral pain visceral pain transmitted by autonomic nervous system via sympathetic fibers from plexuses in close proximity to the viscera them selves Regional anesthetic are commonly used to prevent or minimize these side effect the use of ultra sound nerve block are commonly use as apart of multimodal post operative analgesia The tab block is used to decrease the need of post operative analgesia in patient undergoing abdominal plastic surgery It was found an alternative approach to para vertebral block the retro laminar block is performed with us guided imaging to reduce pain post operative and need analgesia

Registry
clinicaltrials.gov
Start Date
January 15, 2024
End Date
December 15, 2025
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hadeel Elsagheer

Elwakeel street qsm1

Tanta University

Eligibility Criteria

Inclusion Criteria

  • 90patients aged 18/65years of both sexes and asa physical status one two and three undergoing abdominal plastic surgery

Exclusion Criteria

  • patient refusal Patient taking analgesia of chronic illness or have history of substance abuse Patient who are unable to describe their post operative pain Patient with history of coagulabathy Un cooperative patient Patient with known allergy to study drug Patient with infection at site needle puncture Patient with decompensated hepatic renal respiratory or cardiac disorder

Outcomes

Primary Outcomes

Total dose of morphine consumption in the first postoperative 24hours

Time Frame: First 24hours

Total dose of morphine consumption in the first postoperative 24hours

Study Sites (1)

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