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