Deep Parasternal Intercostal Plane Block Versus Erector Spinae Plane Block in Pediatric Cardiac Patients Undergoing Primary Repair of Septal Defects Via Median Sternotomy

ConditionSeptal Defect
Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age1-10
SponsorAin Shams University

About this trial

In this study we are aiming to compare the Erector Spinae Plane Block and the Deep Parasternal intercostal plane block as regard to their technique, application and outcome in order to describe the most suitable method for pediatric cardiac patients undergoing primary repair of septal defects

The primary outcome of this study will be the time of the first request for postoperative analgesics by FLACC pain scale more than 4 The secondary outcomes will be the total postoperative analgesic consumption, time for extubation, the incidence of nausea and vomiting, hemodynamic instability, onset of ambulation and any other complications on the first day after surgery

Participants will be enrolled in this double-blinded randomly allocated using computer-based randomization into three groups. Group 1 will receive bilateral deep parasternal intercostal plane block. Group 2 will receive bilateral erector spinae plane block. Group 3 will receive conventional analgesic regimen without having a regional block

Eligibility criteria

Qualifiers

Pediatric patients with acyanotic heart disease

Patients with septal defect undergoing primary repair

ASA Ⅰ and Ⅱ

Disqualifiers

Patient's guardian refusal of procedure or participation in the study.

Patients with hemodynamic instability

Preexisting infection at the block site

Allergy to local anesthetics

Trial design

Treatments tested in this trial

  • Deep Parasternal intercostal plane block
  • Erector Spinae Plane Block
  • conventional analgesic regimen

Treatment groups

45 Participants
are divided into 3 treatment groups

Sponsors and collaborators