Comparing two anesthesia techniques for upper abdominal surgery
Comparison Between Ultrasound Guided Rhomboid Intercostal Plane Block and Thoracic Erector Spinae Plane Block in Patients Undergoing Upper Abdominal Surgery: A Randomized Controlled Trial
This study tests which of two ultrasound-guided anesthesia techniques can provide better pain relief for patients having upper abdominal surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 21 Years to 65 Years |
| Sex | All |
| Sponsor | Tanta University Academic / other |
| Locations | 1 site (Tanta, El-Gharbia) |
| Trial ID | NCT06654635 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of two ultrasound-guided anesthesia techniques, the rhomboid intercostal plane block and the thoracic erector spinae block, in providing pain relief for patients undergoing upper abdominal surgery. The research aims to determine which technique offers better analgesic efficacy, thereby improving postoperative outcomes. By utilizing ultrasound guidance, the study seeks to enhance the safety and effectiveness of regional anesthesia compared to traditional methods. The findings could lead to improved pain management strategies in surgical settings.
Who should consider this trial
Good fit: Ideal candidates for this study are patients aged 21-65 years, of any gender, classified as ASA I-II, and scheduled for elective upper abdominal surgery.
Not a fit: Patients with chronic pain, significant comorbidities, or those who are obese with a BMI over 35 may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to better pain management and recovery experiences for patients undergoing upper abdominal surgery.
How similar studies have performed: Previous studies have shown promising results with ultrasound-guided regional anesthesia techniques, indicating potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients aged 21-65 years. * Both gender. * American Society of Anesthesiologists (ASA) classification I-II. * Presented for elective upper abdominal surgery. Exclusion Criteria: * Patients refused to participate. * Patients with known or suspected allergy to the used medication. * Patients with preoperative chronic pain. * Patients with major cardiac, renal, respiratory, or hepatic disease. * Patients with potential risk of coagulopathy. * Obese patients with body mass index (BMI) \>35.
Where this trial is running
Tanta, El-Gharbia
- Tanta University — Tanta, El-Gharbia, Egypt (Recruiting)
Study contacts
- Study coordinator: Omima M Eldeeb, Master
- Email: omima.eldeeb@med.tanta.edu.eg
- Phone: 01004584669
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.