Erector Spinae Block Versus Combined Pecto-intercostal and Recto-intercostal Fascial Plane Block in Cardiac Surgery

Launched by TANTA UNIVERSITY · Mar 6, 2025

Keywords

ClinConnect Summary

This clinical trial is studying two different ways to manage pain for patients undergoing heart surgery. Specifically, it compares the effectiveness of a technique called the erector spinae block, which targets a specific area in the back, with another method that combines two different blocks to numb the chest area. The goal is to see which method provides better pain relief after surgery.

To be eligible for this trial, participants need to be between 21 and 65 years old and scheduled for open-heart surgery that involves a specific type of incision in the chest. However, certain people cannot participate, such as those with a history of chronic pain, allergies to local anesthetics, or significant heart and organ issues. If someone joins the trial, they can expect to receive either of the pain management techniques before their surgery and will be monitored to see how well it works for them. This study aims to improve pain management for heart surgery patients, helping them recover more comfortably.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Age from 21 to 65 years.
• • Both sexes.
• • Scheduled for open heart surgery with cardiopulmonary bypass and midline sternotomy.
• Exclusion Criteria:
• • History of chronic pain or Long-term or recent use of opioids.
• • History of allergy to local anesthetic drugs.
• • Ejection fraction of left ventricle less than 30%.
• • History of psychiatric diseases or any neurological disorders.
• • Pre-existing major organ dysfunction as hepatic or renal failure.