Clinical Trials Directory

Trials / Unknown

UnknownNCT05420376

Comparison of Whole Mesh and Split Mesh Use in Laparoscopic Inguinal Hernia Repair

Prospective Comparison of Whole Mesh and Split Mesh Use in Patient Groups Undergoing Laparoscopic Inguinal Hernia Repair

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
Istanbul Training and Research Hospital · Other Government
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

At least 80 patients who will undergo laparoscopic inguinal hernia repair surgery will be randomized into 2 groups. For the patients in the first group, the whole mesh will be laid on the area without being fixed. The patients in the second group will be given a mesh of the same size, but partially divided horizontally and wrapped around the spermatic cord. Demographic data of patients in both groups, quality of life data(Carolinas Comfort Scale) at postoperative 1st, 7th, 30th, 3rd and 6th months, postoperative pain (VAS values), clinical seroma rate, recurrence and other complications will be monitored. When the desired number of patients and follow-up period are reached, the data in the 2 groups will be compared.

Conditions

Interventions

TypeNameDescription
PROCEDURESplit MeshTEP repair of inguinal hernias using either split or whole mesh

Timeline

Start date
2022-06-16
Primary completion
2023-05-16
Completion
2023-06-16
First posted
2022-06-15
Last updated
2022-07-20

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT05420376. Inclusion in this directory is not an endorsement.