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Clinical Trials/NCT05012215
NCT05012215
Unknown
N/A

Ultrasound Guided Thoracic Paravertebral Block Versus Ultrasound Guided Caudal Epidural Block in Pediatric Patients Undergoing Percutaneous Nephrolithotomy

Assiut University1 site in 1 country60 target enrollmentAugust 19, 2021

Overview

Phase
N/A
Intervention
Not specified
Conditions
Kidney Stones
Sponsor
Assiut University
Enrollment
60
Locations
1
Primary Endpoint
Heart rate (beats/minute)
Last Updated
4 years ago

Overview

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

Registry
clinicaltrials.gov
Start Date
August 19, 2021
End Date
March 20, 2022
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hany Mostafa Esmaeil Osman

Principal Investigator

Assiut University

Eligibility Criteria

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

Outcomes

Primary Outcomes

Heart rate (beats/minute)

Time Frame: through the surgery, an average of 2 hours

Blood pressure during surgery in mmHg

Time Frame: through the surgery, an average of 2 hours

The concentration of sevoflurane in %

Time Frame: through the surgery, an average of 2 hours

Postoperative pain using FLACC score

Time Frame: up to 12 hours

Study Sites (1)

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