External Oblique Intercostal Plane Block for Patients Undergoing Upper Abdominal Surgeries
Not Applicable
Completed
- Conditions
- Post Operative Pain
- Interventions
- Other: US-guided external oblique intercostal block
- Registration Number
- NCT06514417
- Lead Sponsor
- Menoufia University
- 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.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 25
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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description external oblique intercostal block US-guided external oblique intercostal block receive US-guided external oblique intercostal block after induction
- Primary Outcome Measures
Name Time Method Visual analogue pain scale . 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 Outcome Measures
Name Time Method total perioperative analgesics requirements 24 hours Milligram
Trial Locations
- Locations (1)
Menoufia university
🇪🇬Cairo, Shibin Elkom, Egypt