Retrolaminar Block Versus Tab Block in Abdomioasty

Not Applicable

Recruiting

• Conditions: Block

• Registration Number: NCT06265402
• Lead Sponsor: Tanta University

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

Study Timeline

• Study Start: 2024-01-15
• Status Verified: 2024-02
• Study First Submitted: 2024-02-11
• Study First Submitted QC: 2024-02-11
• Last Update Submitted: 2024-02-11
• Study First Posted: 2024-02-20
• Last Update Posted: 2024-02-20
• Primary Completion: 2025-10-15
• Study Completion: 2025-12-15

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 90

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Total dose of morphine consumption in the first postoperative 24hours	First 24hours	Total dose of morphine consumption in the first postoperative 24hours

Trial Locations

Locations (1)

TantaU U; 🇪🇬 Tanta, Egypt