New pain management technique for inguinal hernia surgery
Effect of the Quadro-Iliac Plane Block on Quality of Recovery Following Laparoscopic Inguinal Hernia Surgery: A Prospective, Randomized, Controlled, Double-Blind, Multicenter Study
This study is testing a new way to manage pain after inguinal hernia surgery to see if it helps patients recover faster compared to standard pain relief methods.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 70 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Konya City Hospital Academic / other |
| Locations | 1 site (Konya) |
| Trial ID | NCT06862609 on ClinicalTrials.gov |
What this trial studies
This clinical trial investigates the effectiveness of the quadro-iliac plane block for managing postoperative pain in patients undergoing elective unilateral laparoscopic inguinal hernia repair. The study compares this novel regional anesthesia technique to standard pain management approaches, which often rely on opioids and nonsteroidal anti-inflammatory drugs. By utilizing a specific fascial plane block, the trial aims to improve pain control and facilitate quicker recovery and discharge for patients. The study will enroll patients aged 18-65 who are undergoing this common surgical procedure under general anesthesia.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18-65 undergoing elective unilateral laparoscopic inguinal hernia repair under general anesthesia.
Not a fit: Patients who may not benefit from this study include those with contraindications to regional anesthesia, impaired consciousness, or coagulopathy.
Why it matters
Potential benefit: If successful, this approach could significantly enhance postoperative pain management, leading to faster recovery times and improved patient satisfaction.
How similar studies have performed: While the quadro-iliac plane block is a novel approach, similar fascial plane blocks have shown promise in other studies for improving postoperative pain management.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients aged 18-65 years * Undergoing elective, * unilateral laparoscopic inguinal hernia repair * Receiving general anesthesia Exclusion Criteria: * Patients who refuse to provide consent * Patients with contraindications to regional anesthesia * Patients with impaired consciousness * Patients with coagulopathy * Patients with infections at the block site * Emergency cases
Where this trial is running
Konya
- Konya City Hospital — Konya, Turkey (Türkiye) (Recruiting)
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.