Actively Recruiting
EOI Block Versus ESP Block in Laparoscopic Bariatric Surgery
Led by Cairo University · Updated on 2024-05-16
50
Participants Needed
1
Research Sites
25 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study aims to compare a single shot of bilateral ultrasound-guided EOI block and ESPB in terms of intraoperative opioid consumption, postoperative pain control in the first 24 hours, and the need for rescue analgesics.
CONDITIONS
Official Title
EOI Block Versus ESP Block in Laparoscopic Bariatric Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Obese patients of any gender with a body mass index (BMI) of 63 35 kg/m2 with comorbidities or > 40 kg/m2
- American Society of Anesthesiologists (ASA) physical status I-III
- Aged between 18 and 70 years
- Scheduled for laparoscopic bariatric surgery, including sleeve gastrectomy and/or Roux-en-Y gastric bypass (RYGB) surgery
You will not qualify if you...
- Coagulopathy or blood clotting problems
- Infection at the injection site
- Allergy to local anesthetics
- Severe liver or kidney disease
- Severe cardiopulmonary disease (ASA IV or higher)
- Diabetic or other neuropathies
- Receiving opioids for chronic pain treatment
- Unable to understand or use the visual analogue scale (VAS) for pain assessment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Cairo university Hospitals. kasralainy
Cairo, Governorate, Egypt, 002
Actively Recruiting
Research Team
N
Nagy malak
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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