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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06417359
Other study ID # 65656565
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date October 4, 2023
Est. completion date October 4, 2024

Study information

Verified date May 2024
Source Konya City Hospital
Contact Abdullah Hilmi Yilmaz, MD
Phone 0432 222 00 10
Email drabdullahhilmi@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date October 4, 2024
Est. primary completion date April 4, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Mesh Fixation
That mesh will be fixation with three tackers.
No Mesh Fixation
That mesh will not be fixation

Locations

Country Name City State
Turkey University of Health Science Van Training and Research Hospital Van

Sponsors (2)

Lead Sponsor Collaborator
Mehmet Esref Ulutas Van Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

References & Publications (3)

Claus CM, Rocha GM, Campos AC, Bonin EA, Dimbarre D, Loureiro MP, Coelho JC. Prospective, randomized and controlled study of mesh displacement after laparoscopic inguinal repair: fixation versus no fixation of mesh. Surg Endosc. 2016 Mar;30(3):1134-40. do — View Citation

Claus CMP, Rocha GM, Campos ACL, Paulin JAN, Coelho JCU. Mesh Displacement After Bilateral Inguinal Hernia Repair With No Fixation. JSLS. 2017 Jul-Sep;21(3):e2017.00033. doi: 10.4293/JSLS.2017.00033. — View Citation

Yildirim MB, Sahiner IT. The effect of mesh fixation on migration and postoperative pain in laparoscopic TEP repair: prospective randomized double-blinded controlled study. Hernia. 2023 Feb;27(1):63-70. doi: 10.1007/s10029-022-02587-w. Epub 2022 Mar 14. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Status of Mesh Displacement Patients who are suitable for discharge will be discharged after a pelvis x-ray is taken. One month after the surgery and 6 months later, patients will be called to the outpatient clinic and examined and pelvic radiographs will be taken. The movement of the clips marked on the patch will be compared with previous radiographs in cm. postoperative 24 hours, 1 and 6 months
Secondary Rate of Postoperative pain It will be measured using the Visual Analog Score (VAS). The patient will be asked to choose between the number 1 with the least pain and the number 10 with the most pain. The lowest score on this scale is 1, and the highest score is 10. postoperative 24 hours
Secondary Rate of Hernia recurrence hernia recurrence after six months of follow-up. It will be checked by physical examination. Imaging methods will be used in suspicious cases. postoperative 6th month and first year
Secondary Rate of Postoperative complications such as wound infection, bleeding postoperative 24 hours and 1st month
Secondary Rate of Chronic pain It will be measured using the Visual Analog Score (VAS). The patient will be asked to choose between the number 1 with the least pain and the number 10 with the most pain. The lowest score on this scale is 1, and the highest score is 10. postoperative 1st, 6th month and first year
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