Comparing two pain management techniques after umbilical hernia repair
Erector Spinae Plane Block Versus Oblique Subcostal Transverses Abdominis Plane Block for Controlling Postoperative Pain After Umbilical Hernia Repair
This study is testing which pain management technique, either the ESP block or the TAP block, works better for people recovering from umbilical hernia surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 52 (estimated) |
| Ages | 21 Years to 60 Years |
| Sex | All |
| Sponsor | Zagazig University Government |
| Locations | 1 site (Zagazig, Sharkia) |
| Trial ID | NCT05286125 on ClinicalTrials.gov |
What this trial studies
This study compares the effectiveness of two regional anesthesia techniques, the erector spinae plane (ESP) block and the oblique subcostal transverse abdominis plane (TAP) block, in managing postoperative pain following umbilical hernia repair. Patients will be randomly assigned to receive either the ESP block or the TAP block after their surgery. The goal is to determine which technique provides better pain control, potentially leading to improved recovery times and patient satisfaction. The study aims to address the limitations of traditional analgesic methods by utilizing ultrasound-guided regional anesthesia.
Who should consider this trial
Good fit: Ideal candidates are adults aged 21 to 60 scheduled for elective umbilical hernia repair with ASA physical status I or II.
Not a fit: Patients with chronic pain, psychological issues, or contraindications to regional anesthesia 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 umbilical hernia repair.
How similar studies have performed: Previous studies have shown promise in using regional anesthesia techniques for postoperative pain management, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients scheduled for elective umbilical hernia repair. * Patient acceptance. * Both sex * Patient's age 21 - 60 years. * Patients with American Society of Anesthesiologists (ASA) physical status I, II. * BMI 25 - 30 kg m-2. Exclusion Criteria: * Uncooperative patients and patients with psychological problems. * Patients with liver or renal impairment. * Patients with contraindication to regional anesthesia. * Patients with history of allergy to drug used in the study. * Patients with chronic pain.
Where this trial is running
Zagazig, Sharkia
- Zagazig University hospital — Zagazig, Sharkia, Egypt (Recruiting)
Study contacts
- Principal investigator: Michael A shaker, lecturer — Zagazig University
- Study coordinator: michael A shaker, lecturer
- Email: michaeladelshaker@gamil.com
- Phone: 01096457282
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.