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Paravertebral Versus Caudal Block in Pediatric PCNL

Not Applicable
Conditions
Kidney Stones
Percutaneous Nephrolithotomy
Registration Number
NCT05012215
Lead Sponsor
Assiut University
Brief Summary

To compare the efficacy of Ultrasound guided thoracic paravertebral block versus ultrasound guided caudal epidural block in pediatric patients undergoing percutaneous nephrolithotomy

Detailed Description

Percutaneous Nephrolithotomy (PCNL) is a commonly performed surgical procedure for complex upper renal tract calculi. Although the skin incision for PCNL appears small, the intensity of intraoperative and postoperative pain is significant owing to soft tissue injury.

Paravertebral block is the technique of injecting local anesthetics in a space immediately lateral to where the spinal nerves emerge from the intervertebral foramina. This technique is used increasingly for intra-operative and post-operative.

Caudal epidural block involves placing a needle through the sacral hiatus to deliver medications into the epidural space. This approach is used widely used for surgical anesthesia and analgesia in pediatric patients.

this work aims to compare the efficacy of Ultrasound guided thoracic paravertebral block versus ultrasound guided caudal epidural block in pediatric patients undergoing percutaneous nephrolithotomy

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Patients undergoing percutaneous nephrolithotomy
Exclusion Criteria
  • Coagulation disorders
  • Infection at the site of injection
  • Allergy to the local anesthetics used
  • Spinal cord abnormalities or neurological deficits

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Blood pressure during surgery in mmHgthrough the surgery, an average of 2 hours
The concentration of sevoflurane in %through the surgery, an average of 2 hours
Postoperative pain using FLACC scoreup to 12 hours
Heart rate (beats/minute)through the surgery, an average of 2 hours
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Assiut University

🇪🇬

Assiut, Egypt

Assiut University
🇪🇬Assiut, Egypt
Hany M. Osman, M.D.
Contact
+201002414591
hanymeo@aun.edu.eg
Fatma N. Mohamed, M.D.
Contact
fatmanabil2012@gmail.com
Mohamed Anwar, M.D.
Principal Investigator

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