Comparing two surgical methods for fixing recurrent inguinal hernias
Clinical Study of Transabdominal Preperitoneal Approach Versus Open Tension-free Hernia Repair for the Treatment of Recurrent Inguinal Hernia
NA · The Second Affiliated Hospital of Kunming Medical University · NCT06604572
This study is testing which of two surgical methods works better for fixing recurring inguinal hernias to help patients recover with less pain and fewer complications.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 70 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | The Second Affiliated Hospital of Kunming Medical University (other) |
| Locations | 1 site (Kunming, Yunnan) |
| Trial ID | NCT06604572 on ClinicalTrials.gov |
What this trial studies
This study investigates the effectiveness of two surgical techniques, the transabdominal preperitoneal approach (TAPP) and open tension-free repair, for treating recurrent inguinal hernias. Patients are randomly assigned to either the TAPP group or the open repair group, and various outcomes such as operation time, pain levels, and complications are recorded at multiple follow-up points. The goal is to determine which method provides better clinical results and to guide future treatment decisions for recurrent hernias.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older who have been diagnosed with a recurrent inguinal hernia.
Not a fit: Patients with multiple relapses of inguinal hernia or those who cannot complete follow-up after surgery may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could help identify the most effective surgical approach for patients with recurrent inguinal hernias, leading to improved recovery and reduced complications.
How similar studies have performed: Previous studies have explored various surgical techniques for hernia repair, but this specific comparison of TAPP and open repair for recurrent cases is less common, making it a potentially novel approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * age ≥ 18 years * the diagnosis of recurrent inguinal hernia made by ultrasound or computed tomography (CT) during the present visit * ability to tolerate general anesthesia and local anesthesia surgery * all patients and their families agreed to participate in this study and sign relevant informed consent. Exclusion Criteria: * patch infection during the first surgery * multiple (≥ 2) relapses * inability to cooperate to complete follow-up after surgery
Where this trial is running
Kunming, Yunnan
- Clinical study of recurrent inguinal hernia — Kunming, Yunnan, China (RECRUITING)
Study contacts
- Principal investigator: Weiming Li, doctor — The Second Affiliated Hospital of Kunming Medical University
- Study coordinator: Weiming Li
- Email: liweiming49@163.com
- Phone: 13114225597
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: Recurrent Inguinal Hernia