Pain management technique for laparoscopic hiatus hernia repair
The Analgesic Effects of Ultrasound Guided Recto-intercostal Facial Plane Block in Laparoscopic Hiatus Hernia Repair: A Double-Blind Randomized Controlled Study
This study is testing a new pain management technique using ultrasound to help people feel less pain after laparoscopic surgery for a hernia.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 44 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Tanta University Academic / other |
| Locations | 1 site (Tanta, Gharbia) |
| Trial ID | NCT06820216 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of an ultrasound-guided bilateral recto-intercostal fascial plane block for pain relief in patients undergoing laparoscopic hiatus hernia repair. The procedure aims to reduce postoperative pain and minimize the need for systemic analgesics, particularly opioids, which can lead to complications. By blocking specific thoracic nerves, the study seeks to improve patient outcomes during the perioperative period. The approach is designed to enhance recovery and reduce the risk of adverse effects associated with pain management.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 to 65 scheduled for elective laparoscopic hiatus hernia repair with ASA physical status I-II.
Not a fit: Patients with cardiovascular, pulmonary, or neurological diseases, or those with a history of chronic pain or opioid use may not benefit from this study.
Why it matters
Potential benefit: If successful, this technique could significantly improve pain management and recovery for patients undergoing laparoscopic hiatus hernia repair.
How similar studies have performed: Other studies have shown promising results with similar nerve block techniques, suggesting potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age from 18 to 65 years. * American Society of Anesthesiology (ASA) physical status I-II. * Both sexes. * Scheduled for elective elective laparoscopic hiatus hernia repair under general anesthesia. Exclusion Criteria: * Patients with cardiovascular, pulmonary, or neurological diseases. * History of chronic pain or Long-term or recent use of opioids. * Coagulation disorders. * History of allergy to local anesthetic drugs. * History of previous abdominal surgery. * Pregnancy.
Where this trial is running
Tanta, Gharbia
- Tanta University Hospitals — Tanta, Gharbia, Egypt (Recruiting)
Study contacts
- Study coordinator: Marwa A Eloraby, MD
- Email: marwa.elfert@med.tanta.edu.eg
- Phone: 01008618309
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.