Bilateral Ultrasound Guided Superficial Parasternal Intercostal Plane Block Versus Erector Spinae Plane Block

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age6-4
SponsorCairo University

About this trial

Group (A): This group will receive fentanyl infusion at a dose of (0.5μg/kg/h) all through the whole operation plus ultrasound guided bilateral superficial parasternal intercostal Plane block which will be done by injecting 0.4ml/kg (1:1 solution of bupivacaine 0.25% and lidocaine 1%) at each side3.

Group (B): This group will receive fentanyl infusion at a dose of (0.5μg/kg/h) all through the whole operation plus Ultrasound guided bilateral ESPB which will be done by injecting 0.4ml/kg (1:1 solution of bupivacaine 0.25% and lidocaine 1%) at each side .

Eligibility criteria

Qualifiers

RACHS-1: Categories 1, 2 and 3

Patients undergoing corrective cardiac surgeries with midline sternotomy incision.

Redo surgeries.

Disqualifiers

Patients whose parents or legal guardians refuse to participate.

Preoperative mechanical ventilation.

Preoperative inotropic drug infusion.

Coagulopathy.

Trial design

Treatments tested in this trial

  • superficial parasternal intercostal Plane block
  • Erecto spinea plane block

Treatment groups

50 Participants
are divided into 2 treatment groups

Sponsors and collaborators