RecruitingNot Applicable

Ultrasound Guided Paravertebral Block Versus Erector Spinae Block for Postoperative Analgesia After Inguinal Hernia Repair in Pediatric Patients

Egypt158 participantsStarted 2024-12-30

Plain-language summary

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.

Who can participate

Age range24 Months – 12 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: 1 - Parents acceptance 2\. Age: preschool and school age child (24 months-12 years old). 3\. Sex: both sex (males or females). 4\. Physical status: ASA 1\& II. 5\. Type of operation: elective unilateral inguinal hernia repair Exclusion Criteria: 1- Patient with any contraindications of regional blocks (as coagulopathy or local infection at injection site) 2\. Patients with known history of allergy to the study drugs (bupivacaine and lidocaine). 3\. Advanced hepatic, renal, cardiovascular, neurologic and respiratory diseases.

What they're measuring

The total amount of rescue analgesia (Ibuprofen consumption)

Timeframe: for 24 hours postoperative

Trial details

NCT IDNCT06752252

SponsorZagazig University

Sponsor typeOTHER_GOV

Study typeINTERVENTIONAL

Primary completion2025-09-30

Contact for this trial

Dina Sadek Salem, MD

0109933513 dinamaghraby@yahoo.com

View on ClinicalTrials.gov More Analgesia, Postoperative trials