Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT07366138

Ultrasound-Guided External Oblique Intercostal Plane Block Versus Subcostal Transversus Abdominis Plane Block For Perioperative Analgesia in Laparoscopic Sleeve Gastrectomy

Led by Benha University · Updated on 2026-01-26

70

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to compare the analgesic efficacy, duration of analgesia, and overall opioid consumption between the external oblique intercostal plane (EOIP) block and subcostal transversus abdominis plane (TAP) block in patients undergoing laparoscopic sleeve gastrectomy.

CONDITIONS

Official Title

Ultrasound-Guided External Oblique Intercostal Plane Block Versus Subcostal Transversus Abdominis Plane Block For Perioperative Analgesia in Laparoscopic Sleeve Gastrectomy

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age from 18 to 65 years
  • Both genders
  • American Society of Anesthesiologists (ASA) class I or II
  • Body mass index (BMI) between 30-50 kg/m8
  • Scheduled for elective laparoscopic sleeve gastrectomy under general anesthesia
  • Written informed consent from patients or surrogate decision makers
Not Eligible

You will not qualify if you...

  • Patient refusal
  • Allergy to local anesthetics
  • Coagulation disorders or anticoagulant therapy
  • Local infection or scar at the injection site
  • Severe hepatic or renal dysfunction
  • Chronic opioid use or psychiatric illness interfering with pain assessment
  • Conversion to open surgery or intraoperative complications requiring re-exploration

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Benha University

Banhā, Benha, Egypt, 13518

Actively Recruiting

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Research Team

A

Ahmed A Ali, MBBCH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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