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NCT04690894

Erector Spinae Muscle Block Versus Caudal Block by Sonar in Pediatrics Undergoing Lower Abdominal Surgery

Completed NA Last updated 8 March 2021
What this trial tests

NA trial testing erector spinae block - caudal block in Postoperative Analgesia in 60 participants. Completed in 15 February 2020.

Timeline
15 July 2019
Primary endpoint
15 January 2020
15 February 2020

Quick facts

Lead sponsorMinia University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment60
Start date15 July 2019
Primary completion15 January 2020
Estimated completion15 February 2020
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Minia University

Who can join

Adults 2 to 6, any sex, with Postoperative Analgesia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

this prospective randomized double blind controlled study was conducted on 60 child scheduled for lower abdominal surgery under general anesthesia. the patients were randomly allocated into 3 parallel groups.group (ESB) patients received ultrasound-guided erector spinae block in a dose of 0.4mg/ml of 0.25%bupivacaine between the 10th transverse process and erector spinae muscles.group(CB) patients received ultrasound-guided caudal block in a dose of 2.5mg/kg of 0.25%bupivacaine. group(CO) did,t received any block

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Postoperative Analgesia

Currently open trials in the same condition.

Other Minia University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04690894.

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