Comparing two pain relief techniques for heart surgery
Analgesic Efficacy of Erector Spinae Plane Block Versus Combined Pecto-intercostal and Recto-intercostal Fascial Plane Block in Patients Undergoing Cardiac Surgery: A Randomized Comparative Trial
This study is testing which of two pain relief methods is better for helping heart surgery patients feel less pain after their operation.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 66 (estimated) |
| Ages | 21 Years to 65 Years |
| Sex | All |
| Sponsor | Tanta University Academic / other |
| Locations | 1 site (Tanta, Gharbia Governorate) |
| Trial ID | NCT06870383 on ClinicalTrials.gov |
What this trial studies
This study aims to compare the effectiveness of two regional anesthesia techniques, the erector spinae plane block and the combined pecto-intercostal and recto-intercostal fascial plane block, in managing postoperative pain for patients undergoing cardiac surgery. The research will utilize ultrasound guidance to administer these blocks and assess their analgesic effects. Given the high incidence of severe pain following median sternotomy, this study seeks to identify which technique provides better pain control. The findings could enhance postoperative care and improve patient outcomes in cardiac surgery.
Who should consider this trial
Good fit: Ideal candidates are adults aged 21 to 65 scheduled for open heart surgery with midline sternotomy.
Not a fit: Patients with chronic pain, recent opioid use, or significant organ dysfunction may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for patients undergoing cardiac surgery.
How similar studies have performed: Previous studies have shown promising results for similar regional anesthesia techniques, suggesting potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion 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.
Where this trial is running
Tanta, Gharbia Governorate
- Tanta University Hospitals — Tanta, Gharbia Governorate, Egypt (Recruiting)
Study contacts
- Study coordinator: Osama M Rehab, MD
- Email: osamarehab@med.tanta.edu.eg
- Phone: 01095210806
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.