Ultrasound Guided Quadratus Lumborum Block Compared to Caudal Bupivacaine/ Neostigmine in Pediatric Lower Abdominal Surgeries
NCT ID: NCT04720287
Last Updated: 2021-05-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE4
60 participants
INTERVENTIONAL
2021-02-01
2021-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
DOUBLE
Study Groups
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Group 1(QL group)
bupivacaine/ neostigmine.
will receive bilateral ultrasound guided QLB
Group 2 (CB group)
bupivacaine/ neostigmine.
will receive ultrasound guided CB.
Interventions
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bupivacaine/ neostigmine.
will receive bilateral ultrasound guided QLB
bupivacaine/ neostigmine.
will receive ultrasound guided CB.
Eligibility Criteria
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Inclusion Criteria
* Consent from parents or legal guardian(s).
* Lower abdominal surgeries.
Exclusion Criteria
* Infection at the injection site.
* Known allergy to bupivacaine and/or neostigmine.
* Contraindications to regional anesthesia (including coagulopathy and local infection).
* Anatomical anomalies at the site of the block.
15 Years
ALL
No
Sponsors
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Ain Shams University
OTHER
Responsible Party
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Dr.Ibrahim Mamdouh Esmat
Assistant Professor of Anesthesia and Intensive Care Department, Faculty of Medicine, Ain- shams University, Cairo, Egypt.
Locations
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Ain-Shams University Hospitals
Cairo, , Egypt
Countries
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Other Identifiers
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FMASU MS 728/2020/2021
Identifier Type: -
Identifier Source: org_study_id
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