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

Trial statusRecruiting
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

This trial does not accept healthy volunteers

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

Design model

Parallel

Treatments tested in this trial

  • superficial parasternal intercostal Plane block

    Procedure/Surgery

    A high-frequency linear transducer was used to guide the insertion of a needle 2 cm lateral to the sternum. After identifying key anatomical structures, the needle was advanced in-plane into the pectointercostal fascial plane between the pectoralis major and internal intercostal muscle. Correct placement was confirmed with a saline injection, and then a local anesthetic (0.4 ml/kg of a 1:1 mix of bupivacaine 0.25% and lidocaine 1%) was injected bilaterally at the second and fourth ribs.

  • Erecto spinea plane block

    Procedure/Surgery

    Using ultrasound, a needle is inserted near the T5 vertebra into the plane beneath the erector spinae muscle. After confirming correct positioning with saline, a local anesthetic mixture is injected in the fascial plane.

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: Superficial parasternal intercostal Plane block groupExperimental treatment 1 intervention
Group B: Erecto-Spinea plane block groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Pain assessment

Pain was assessed by the pediatric observational 10-point scale "Face, Leg, Activity, Cry, Consolability (FLACC) pain score.

Time frame
Immediately after admission to ICU then at 60 min, 2 hours, 4 hours, 8 hours and 12 hours postoperatively

Secondary outcomes

Other outcomes

Sponsors and contacts

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