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NCT04720287 Clinical Trial

Ultrasound Guided Quadratus Lumborum Block Compared to Caudal Bupivacaine/ Neostigmine in Pediatric Lower Abdominal Surgeries

Postoperative Analgesia Clinical Trial

Official title:
Ultrasound Guided Quadratus Lumborum Block Compared to Caudal Bupivacaine/ Neostigmine in Pediatric Lower Abdominal Surgeries, a Randomized Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04720287
Other study ID # FMASU MS 728/2020/2021
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date February 1, 2021
Est. completion date April 30, 2021

Study information
Verified date May 2021
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to compare the postoperative pain control in children undergoing lower abdominal surgeries receiving QL block with those receiving caudal bupivacaine/ neostigmine.

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date April 30, 2021
Est. primary completion date April 30, 2021
Accepts healthy volunteers No
Gender All
Age group N/A to 15 Years
Eligibility Inclusion Criteria: - Patients American Society of Anesthesiologists physical status (ASA) I or II. - Consent from parents or legal guardian(s). - Lower abdominal surgeries. Exclusion Criteria: - Parents' refusal or legal guardian's refusal. - 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.

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• bupivacaine/ neostigmine.
will receive bilateral ultrasound guided QLB
• bupivacaine/ neostigmine.
will receive ultrasound guided CB.

Locations
Country Name City State
Egypt Ain-Shams University Hospitals Cairo

Sponsors (1)
Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary The total amount of paracetamol doses (mg) The total amount of paracetamol doses (mg) 24 hours postoperatively
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