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Clinical Trials/NCT04518215
NCT04518215
Completed
Not Applicable

Ultrasound-Guided Erector Spinae Plane Block for Paediatric Upper Abdominal Surgery: A Randomized Controlled Study

Nazmy Edward Seif1 site in 1 country40 target enrollmentAugust 20, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Paediatric
Sponsor
Nazmy Edward Seif
Enrollment
40
Locations
1
Primary Endpoint
Tramadol consumption.
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Upper abdominal surgeries are associated with severe postoperative pain. Thus, maintaining effective postoperative analgesia in the paediatric age group is very crucial in terms of future pain perception and chronic pain development. Erector Spinae Plane Block (ESPB) is an interfascial plane block characterized by its ease of application and low complication rates with the introduction of ultrasonography. The aim of this study is to investigate the analgesic effects of ESPB in this particular age-group.

Registry
clinicaltrials.gov
Start Date
August 20, 2020
End Date
December 15, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Nazmy Edward Seif
Responsible Party
Sponsor Investigator
Principal Investigator

Nazmy Edward Seif

Clinical Professor

Cairo University

Eligibility Criteria

Inclusion Criteria

  • ASA I - II.
  • Elective open upper abdominal surgeries, e.g., open cholecystectomy, splenectomy, pyeloplasty, renal cysts excision, partial or total nephrectomy.

Exclusion Criteria

  • Patient's next of kin refusal.
  • Allergy to local anaesthetics.
  • Infection at the site of injection.
  • Coagulopathy.

Outcomes

Primary Outcomes

Tramadol consumption.

Time Frame: 24 hours

Total dose of Tramadol (measured in mg) given intra-venously to the patient post-operatively.

Study Sites (1)

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