NOL-Guided Superficial Parasternal Intercostal Plane Block Versus Erector Spinae Plane Block

• Status: Completed
• Trial end date: 2024-04-01
• Target enrollment: 0
• Participant gender: All

Summary

This clinical trial focuses on an elaborate, propensity-matched, non-inferiority comparison of NOL-guided Superficial Parasternal Intercostal Plane Block (SPIPB) and Erector Spinae Plane Block (ESPB) within the context of open-heart surgery with cardiopulmonary bypass.

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Institutul de Urgenţă pentru Boli Cardiovasculare Prof.Dr. C.C. Iliescu
• Treatments: Anesthetics; Anesthetics, General; Morphine

Criteria

Inclusion Criteria:

1. Informed Consent.

2. Elective heart surgery with sternotomy and bypass.

3. Hemodynamic stability prior to induction.

4. Sinus rhythm.

Exclusion Criteria:

1. Known allergy to any of the medications used in the study.

2. BMI > 35.

3. Patient refusal to participate in the study.

4. Coagulopathy (INR > 1.5, APTT > 45, Fibrinogen < 150 mg/dl).

5. Non-elective/emergent and/or redo surgery.

6. ASA ≥ 4.

7. Any preoperative hemodynamic support (mechanical or pharmaceutical).

8. Severe LV dysfunction (LVEF ≤ 30%).

9. Severe RV dysfunction.