Comparing two types of nerve blocks for pain relief after abdominal surgery
Is Erector Spinae Plane Block More Effective Than Rectus Sheath Block for Postoperative Analgesia After Supraumbilical Surgery in Adult Patients
This study is testing which type of nerve block, the erector spinae plane block or the rectus sheath block, works better for pain relief after abdominal surgery to help adults recover with less need for opioids.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 21 Years to 60 Years |
| Sex | All |
| Sponsor | Damanhour Teaching Hospital Government |
| Locations | 1 site (Damanhūr, El-Beheira) |
| Trial ID | NCT05179928 on ClinicalTrials.gov |
What this trial studies
This study aims to compare the effectiveness of the erector spinae plane block (ESPB) and the rectus sheath block (RSB) in providing postoperative pain relief for adult patients undergoing supraumbilical surgery. The focus is on reducing the need for opioids, which can have adverse side effects, by utilizing regional analgesic techniques. The study will evaluate patient outcomes related to pain management and overall recovery following surgery.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 21 to 60 years with an ASA physical status of II or less and a BMI under 35 kg/m².
Not a fit: Patients who may not benefit from this study include those with severe comorbidities, altered mental status, or those outside the specified age and BMI criteria.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies that minimize opioid use after surgery.
How similar studies have performed: Previous studies have indicated that regional analgesic techniques like ESPB and RSB can effectively manage postoperative pain with fewer side effects, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * American Society of Anesthesiologists (ASA) physical status ≤ II * Age from 21 to 60 years * Body Mass Index (BMI) \< 35 kg/m² Exclusion Criteria: * American Society of Anesthesiologists (ASA) physical status \> II * Age \< 21 years or \> 60 years * Body Mass Index (BMI) ≥ 35 * Local infection at the puncture site * Altered mental status * Pregnant women * Allergy to study drugs * Chronic pain * Coagulation abnormalities or on anticoagulants * Severe hepatic or kidney disease
Where this trial is running
Damanhūr, El-Beheira
- Damanhour Teaching Hospital — Damanhūr, El-Beheira, Egypt (Recruiting)
Study contacts
- Principal investigator: Ahmed M Shaat, MD — Damanhour Teaching Hospital
- Study coordinator: Ahmed M Shaat, MD
- Email: ahmedshaat99@gmail.com
- Phone: 00201223482709
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.