Actively Recruiting
Comparison of Mesh Fixation and Non-Fixation in eTEP
Led by Mehmet Eşref Ulutaş · Updated on 2024-05-24
60
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
Sponsors
M
Mehmet Eşref Ulutaş
Lead Sponsor
V
Van Training and Research Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
Inguinal hernia surgery is one of the most frequently performed procedures among general surgery cases. As with many open surgical methods, this repair is also performed laparoscopically. Among these closed methods, the one method is laparoscopic extended total extraperitoneal repair (eTEP). The benefits of laparoscope include less postoperative pain and complications, faster recovery, reduced chronic pain, and recurrence rate. One of the recent debates regarding the laparoscopic technique is mesh fixation. Fixation of the mesh to the cooper ligament can prevent mesh migration and consequently reduce the recurrence rate. However, it has been reported that this fixation may increase postoperative pain. Several studies have reported that recurrence may be due to inadequate mesh fixation technique. In contrast, other prospective randomized studies have found relapse unrelated to mesh fixation. In the eTEP technique, dissection is performed in a larger area than in TEP. For this reason, it can be thought that the possibility of mesh displacement is higher in the eTEP procedure. The purpose of this study is to confirm this idea with a prospective study. There are studies in the literature on mesh fixation related to the total extraperitoneal repair (TEP) technique. However, there is no study on mesh detection in the eTEP technique. The aim of the study is to compare patients who underwent withmesh fixation and without mesh fixation laparoscopic eTEP repair in terms of clinical data such as mesh displacement and hernia recurrence, chronic pain, length of hospital stay, and postoperative complications.
CONDITIONS
Official Title
Comparison of Mesh Fixation and Non-Fixation in eTEP
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with unilateral inguinal hernias
- Patients aged 18-65
You will not qualify if you...
- 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
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Health Science Van Training and Research Hospital
Van, Turkey (Türkiye)
Actively Recruiting
Research Team
A
Abdullah Hilmi Yılmaz, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here