Comparing two techniques for inguinal hernia repair
Comparative Study of Modified Guarnieri-Desarda Technique Versus Lichtenstein Technique in Inguinal Hernia Repair
NA · Cairo University · NCT06595628
This study is testing two different surgical methods for fixing inguinal hernias in adult men to see which one leads to less pain and fewer complications after surgery.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 18 Years and up |
| Sex | Male |
| Sponsor | Cairo University (other) |
| Locations | 1 site (Cairo) |
| Trial ID | NCT06595628 on ClinicalTrials.gov |
What this trial studies
This study aims to compare the surgical outcomes of the Lichtenstein tension-free mesh hernioplasty technique with the combined modified Guarnieri-Desarda technique for inguinal hernia repair. It will evaluate postoperative pain, complications such as seroma and infection, chronic inguinodenia, early recurrence rates, and testicular vascularity and size using duplex ultrasound. Adult male patients with non-complicated inguinal hernias will be recruited for this interventional study.
Who should consider this trial
Good fit: Ideal candidates for this study are adult males aged 18 years or older with non-complicated inguinal hernias.
Not a fit: Patients with complicated hernias or those with a history of prior inguinal surgery may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved surgical outcomes and reduced complications for patients undergoing inguinal hernia repair.
How similar studies have performed: While there have been various techniques for hernia repair, the specific comparison of these two techniques has not been extensively tested, making this a novel approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult male patients aged 18 years or older. * Patients diagnosed with non-complicated inguinal hernia (both direct and indirect). * Patients able to provide written informed consent to participate in the study. Exclusion Criteria: * Patients younger than 18 years old. * Patients with complicated hernias (e.g., inflamed, obstructed, or strangulated hernias). * Patients with a recurrent inguinal hernia. * Patients with weak or thin external oblique aponeurosis (intraoperative findings). * Patients with a history of prior surgery in the inguinal region. * Patients who refuse to participate in the study.
Where this trial is running
Cairo
- Kasralainy — Cairo, Egypt (RECRUITING)
Study contacts
- Principal investigator: Fadi F. Khalil, MSc — Kasr El Aini Hospital
- Study coordinator: Fadi F. Khalil, MSc
- Email: fady.azmi37080@postgrad.kasralainy.edu.eg
- Phone: 01285612963
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.
Conditions: Inguinal Hernia, Hernia Repair, Guarnieri Technique, Desarda Technique, Lichtenstein Hernioplasty