Comparing two techniques for repairing inguinal hernias
Comparative Study Between Desarda's Technique Versus Lichtenstein's Technique Hernia Repair in Management of Elective Non-complicated Inguinal Hernia (Randomized Controlled Trial)
This study is testing two different ways to fix inguinal hernias to see which one is safer and leads to better recovery for patients.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 200 (estimated) |
| Ages | 14 Years and up |
| Sex | All |
| Sponsor | Minia University Academic / other |
| Locations | 1 site (Minya, Minya Governorate) |
| Trial ID | NCT06862167 on ClinicalTrials.gov |
What this trial studies
This study compares Desarda's technique and Lichtenstein's technique for repairing elective, non-complicated inguinal hernias. The Desarda technique avoids the use of mesh, which can lead to complications such as chronic pain and infection, while the Lichtenstein technique involves mesh implantation. The study aims to evaluate the effectiveness and safety of both methods in terms of recurrence rates and patient outcomes. Participants will be monitored for complications and recovery following their respective procedures.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals aged 14 and older with reducible, non-complicated inguinal or inguinoscrotal hernias.
Not a fit: Patients with obstructive uropathy, chronic obstructive pulmonary disease, or those unfit for surgery may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a safer and more effective hernia repair option that minimizes complications associated with mesh use.
How similar studies have performed: While the use of mesh in hernia repair is well-established, the Desarda technique is less commonly used and may offer a novel approach to hernia management.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Above 14 years of age. * With reducible non-complicated inguinal or inguinoscrotal hernia; unilateral or bilateral Exclusion Criteria: * Obstructive uropathy or chronic obstructive pulmonary disease because they are contraindications to elective hernia surgery. They are associated with definite poor outcomes, such as high recurrence rates. * Unfit patients for surgery * Patients with strangulated hernia. * Recurrent Hernias. * Per operative finding of separated, thin, and/or weak external oblique aponeurosis
Where this trial is running
Minya, Minya Governorate
- Minia University — Minya, Minya Governorate, Egypt (Recruiting)
Study contacts
- Study coordinator: Abdelrahman M Salah, MD
- Email: Abdelrahman.salah@mu.edu.eg
- Phone: 00201064746493
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.