Comparing conventional and robot-assisted methods for inguinal hernia repair
Conventional Versus Robot Assisted Laparoscopic Inguinal Hernia Repair
This study is testing whether using robot-assisted surgery for inguinal hernia repair helps adults recover faster compared to traditional laparoscopic surgery, especially when local anesthetic is added.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 200 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Algemeen Ziekenhuis Maria Middelares Academic / other |
| Locations | 1 site (Ghent) |
| Trial ID | NCT03904888 on ClinicalTrials.gov |
What this trial studies
This study evaluates the early postoperative outcomes of patients undergoing laparoscopic inguinal hernia repair using either a conventional laparoscopic approach or a robot-assisted technique. It aims to determine if the addition of local anesthetic injections at the trocar wounds improves recovery. The research focuses on adult patients with bilateral inguinal hernias, comparing the effectiveness and recovery times of the two surgical methods. The study is conducted at the Hernia Center Maria Middelares, which has extensive experience with these techniques.
Who should consider this trial
Good fit: Ideal candidates are adult patients with bilateral inguinal hernias who are scheduled for minimally invasive laparoscopic repair.
Not a fit: Patients with unilateral hernias, incarcerated hernias, or those who do not meet the inclusion criteria will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved recovery times and reduced postoperative pain for patients undergoing inguinal hernia repair.
How similar studies have performed: Previous studies have shown promising results with both conventional and robot-assisted laparoscopic techniques, but this specific comparison is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * adult patients presenting with a bilateral inguinal hernia planned for a minimal invasive laparoscopic repair Exclusion Criteria: * Age below 18 years * unilateral groin hernia repair * incarcerated hernias * open hernia repair * no informed consent * pregnant women * ASA score 4 or more * patient included in another study.
Where this trial is running
Ghent
- AZ Maria Middelares — Ghent, Belgium (Recruiting)
Study contacts
- Principal investigator: Filip Muysoms, MD,PhD — Algemeen Ziekenhuis Maria Middelares
- Study coordinator: Filip Muysoms, MD,PhD
- Email: filip.muysoms@gmail.com
- Phone: +32477325710
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.