Pain relief method for epigastric hernia repair
Efficacy and Safety of Bilateral Recto-Intercostal Fascial Plane Block on Perioperative Analgesia in Epigastric Hernia Repair : A Randomized Controlled Trial
This study is testing a new pain relief method for adults having surgery to fix an epigastric hernia to see if it helps reduce pain after the operation.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Tanta University Academic / other |
| Locations | 1 site (Tanta, El-Gharbia) |
| Trial ID | NCT06092073 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness and safety of a bilateral recto-intercostal fascial plane block (RIFPB) for patients undergoing epigastric hernia repair. The RIFPB technique involves injecting a local anesthetic into a specific area near the xiphoid process to block pain signals from the anterior branches of the nerves. The goal is to reduce postoperative pain, which is a common issue following hernia repair surgery. The study will include patients aged 18-65 who are scheduled for elective surgery and meet specific health criteria.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18-65 with ASA physical status I-II scheduled for elective epigastric hernia repair.
Not a fit: Patients with a BMI over 35, large hernias containing bowel, or allergies to local anesthetics may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce postoperative pain for patients undergoing epigastric hernia repair.
How similar studies have performed: While the RIFPB technique is novel, similar regional anesthesia approaches have shown promise in reducing postoperative pain in other surgical contexts.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age 18-65 years. * Both sexes. * American Society of Anesthesiology (ASA) physical status I-II. * Scheduled for elective epigastric hernia repair. Exclusion Criteria: * Obese patients with body mass index (BMI) \>35 kg/m2. * Patients with a large hernia containing bowel. * Patients with local anesthetic allergy.
Where this trial is running
Tanta, El-Gharbia
- Tanta University — Tanta, El-Gharbia, Egypt (Recruiting)
Study contacts
- Study coordinator: Mohammed S ElSharkawy, MD
- Email: mselsharkawy@med.tanta.edu.eg
- Phone: 00201021559948
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.