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Clinical Trials/NCT06514417
NCT06514417
Completed
Not Applicable

Efficacy of Ultrasound - Guided External Oblique Intercostal Plane Block for Patients Undergoing Upper Abdominal Surgeries: A Randomized Controlled Trial

Menoufia University1 site in 1 country25 target enrollmentJuly 10, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Post Operative Pain
Sponsor
Menoufia University
Enrollment
25
Locations
1
Primary Endpoint
Visual analogue pain scale .
Status
Completed
Last Updated
last year

Overview

Brief Summary

Ithe study will evaluate the analgesic efficacy of external oblique intercostal block for patients undergoing upper abdominal surgeries

Detailed Description

Patients will be randomly divided into two equal groups using SPSS. Group A: will receive US-guided external oblique intercostal block after induction Group B: will receive postoperative morphine on patient request. Study design: prospective controlled randomized study.

Registry
clinicaltrials.gov
Start Date
July 10, 2023
End Date
June 10, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Amal Gouda Elsayed Safan

lecturer of anaethesia

Menoufia University

Eligibility Criteria

Inclusion Criteria

  • Selected patients will be more than 21 years old with ASA physical status I \& II scheduled for upper abdominal surgeries

Exclusion Criteria

  • Uncooperative patients.
  • Patients who have allergy to any of the used drugs.
  • Patients who are on opioids.
  • Known abuse of alcohol or medication.
  • Local infection at the site of injection or systemic infection.
  • Pregnancy
  • Patients with coagulation disorders or on anticoagulation therapy

Outcomes

Primary Outcomes

Visual analogue pain scale .

Time Frame: 24 hours

postoperative pain that evaluated by visual analogue pain scale(a scale from 0 to 10 where 0 is interpreted as no pain, 1-4 mild pain, 5-6 moderate pain, 7-10 severe pain)

Secondary Outcomes

  • total perioperative analgesics requirements(24 hours)

Study Sites (1)

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