Actively Recruiting
Ultrasound Guided Paravertebral Block Versus Erector Spinae Block for Postoperative Analgesia After Inguinal Hernia Repair in Pediatric Patients
Led by Zagazig University · Updated on 2025-01-01
158
Participants Needed
2
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of the study is to compare postoperative analgesia in pediatric patients undergoing inguinal hernia repair by comparing the efficacy of ultrasound guided paravertebral block versus ultrasound guided erector spinae plane block.
CONDITIONS
Official Title
Ultrasound Guided Paravertebral Block Versus Erector Spinae Block for Postoperative Analgesia After Inguinal Hernia Repair in Pediatric Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Parents acceptance
- Children aged 24 months to 12 years
- Both males and females
- Physical status classified as ASA 1 or II
- Elective unilateral inguinal hernia repair surgery
You will not qualify if you...
- Contraindications to regional blocks such as bleeding problems or infection at the injection site
- Known allergy to bupivacaine or lidocaine
- Advanced liver, kidney, heart, neurological, or respiratory diseases
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
faculty of human medicine, Zagazig university hospitals
El Sharkia, Egypt
Actively Recruiting
2
Faculty of Human Medicine, Zagazig University
El Sharkia, Egypt
Actively Recruiting
Research Team
D
Dina Sadek Salem, MD
CONTACT
F
Fatima Ahmed, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here