Comparing mesh fixation methods in inguinal hernia surgery
Comparison of Mesh Fixation and Non-Fixation in Laparoscopic eTEP Inguinal Hernia Repair
NA · Konya City Hospital · NCT06417359
This study tests whether using mesh to fix inguinal hernias during surgery can lower the chances of the hernia coming back and reduce pain compared to not using mesh.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Konya City Hospital (other) |
| Locations | 1 site (Van) |
| Trial ID | NCT06417359 on ClinicalTrials.gov |
What this trial studies
This clinical trial investigates the effects of mesh fixation versus no fixation during laparoscopic extended total extraperitoneal repair (eTEP) for inguinal hernias. The study aims to determine whether mesh fixation can reduce implant migration and recurrence rates while assessing its impact on postoperative pain and complications. By comparing these two approaches, the trial seeks to provide insights into the optimal technique for hernia repair. Participants will be monitored for pain levels, complications, and hernia recurrence following surgery.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18-65 with unilateral inguinal hernias.
Not a fit: Patients with bilateral hernias, incarcerated or strangulated hernias, or those contraindicated for general anesthesia may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved surgical outcomes and reduced pain for patients undergoing inguinal hernia repair.
How similar studies have performed: Previous studies have shown mixed results regarding mesh fixation techniques, indicating that this approach is still under investigation.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients with unilateral inguinal hernias, * Patients aged 18-65. Exclusion Criteria: * Younger than 18 years, and older than 65 years, * Incarcerated or strangulated inguinal hernias, * Patients with bilateral inguinal hernias, * Patients who are contraindicated to receive general anesthesia, * Pregnancy
Where this trial is running
Van
- University of Health Science Van Training and Research Hospital — Van, Turkey (Türkiye) (RECRUITING)
Study contacts
- Study coordinator: Abdullah Hilmi Yılmaz, MD
- Email: drabdullahhilmi@gmail.com
- Phone: 0432 222 00 10
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: Migration of Implant, Pain, Postoperative Complications, Relapse