Pain management technique for laparoscopic inguinal hernia repair
Evaluation of the Effectiveness of Transversalis Fascia Plane Block in Patients Undergoing Laparoscopic Inguinal Hernia Repair
This study is testing a new pain management technique using a special injection to see if it can help people feel better and recover faster after laparoscopic inguinal hernia surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Istanbul Medipol University Hospital Academic / other |
| Locations | 1 site (Istanbul, Bagcilar) |
| Trial ID | NCT06778629 on ClinicalTrials.gov |
What this trial studies
This study investigates the effectiveness of the Transversalis Fascia Plane Block (TFPB) in managing postoperative pain following laparoscopic inguinal hernia repair. The TFPB involves injecting local anesthetic between the transversus abdominis muscle and transversalis fascia to block specific spinal nerves. By utilizing ultrasound guidance, the study aims to enhance pain control and reduce reliance on opioids, which can have adverse effects. The goal is to improve recovery times and overall patient comfort after surgery.
Who should consider this trial
Good fit: Ideal candidates for this study are patients classified as ASA I-II who are undergoing elective unilateral inguinal hernia repair.
Not a fit: Patients with chronic pain, allergies to local anesthetics, or certain comorbidities may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce postoperative pain and improve recovery for patients undergoing laparoscopic inguinal hernia repair.
How similar studies have performed: Previous studies have shown positive outcomes with similar interfascial plane blocks for postoperative pain management, indicating a promising approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * American Society of Anesthesiologists (ASA) classification I- II Patients * Unilateral Inguinal Hernia Repair Surgery * Elective Operations Exclusion Criteria: * Patients with a history of chronic pain * Evidence of infection in the intervention area * Allergy to local anesthetics * Coagulopathy * Body-mass index (BMI) ≥ 30 * Body weight ≤ 50 kg * Patients who do not agree to participate in the study
Where this trial is running
Istanbul, Bagcilar
- Istanbul Medipol University Mega Hospital Complex — Istanbul, Bagcilar, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: AYSE INCE, Assist Prof
- Email: drayseince@gmail.com
- Phone: +90 5366774988
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.