Comparing two techniques for inguinal hernia repair
Official title: Comparative Study of Modified Guarnieri-Desarda Technique Versus Lichtenstein Technique in Inguinal Hernia Repair
Run by Cairo University · NCT06595628 · Data updated 2026-11-12
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
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Men only |
| Enrollment | 40 (estimated) |
| Sponsor | Cairo University Academic / other |
| Locations | 1 site (Cairo) |
| Status | Recruiting |
| Started | October 10, 2024 |
| Main results expected | October 1, 2025 |
| Study ends | October 1, 2025 |
| Registry record updated | March 14, 2025 |
| Trial ID | NCT06595628 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adult males aged 18 years or older with non-complicated inguinal hernias.
✕Probably not a fit
Patients with complicated hernias or those with a history of prior inguinal surgery may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
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.
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 gone: 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.
Who can join: the full rules
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 it's running
-
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
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Two laparoscopic techniques for repairing inguinal hernias in children
This study tests whether LPEC or LIS works better for repairing inguinal hernias in children aged 1 to 15 who need laparoscopic repair.
-
Shouldice groin hernia repair: permanent vs slowly dissolving stitches
We’re testing whether slowly dissolving stitches (PDS) work as well as permanent stitches (Prolene) for adults with a non-mesh Shouldice inguinal hernia repair.
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Acupressure for Postoperative Pain After Laparoscopic TEP Hernia Repair
This trial tests whether true acupressure, given after surgery, reduces pain more than sham acupressure or standard care for adults undergoing laparoscopic TEP inguinal hernia repair.
-
TREPP: A Minimally Invasive Open Approach to Repair Inguinal Hernias
This study tests the trans rectus sheath extra-peritoneal procedure (TREPP) to repair inguinal hernias and see if it reduces pain and recurrence relative to traditional methods.
-
Camera-based non-contact vital sign monitoring during surgery
This project will try a camera-based non-contact system to measure heart rate, blood pressure, and oxygen levels in adults having surgery under general anesthesia.
-
Pneumoperitoneum time and bicarbonate changes during laparoscopic inguinal hernia repair
This study will see if longer pneumoperitoneum time during laparoscopic inguinal hernia repair causes changes in blood bicarbonate levels in adults.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.