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Clinical Trials/NCT02023203
NCT02023203
Completed
Not Applicable

Prospective Randomized Clinical Trial Comparing Microporous Polypropylene Mesh and Flexible Macroporous Polytetrafluoroethylene Mesh in Totally Extraperitoneal Laparoscopic Inguinal Hernia Repair

Hospitales Universitarios Virgen del Rocío1 site in 1 country100 target enrollmentJanuary 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hernia, Inguinal
Sponsor
Hospitales Universitarios Virgen del Rocío
Enrollment
100
Locations
1
Primary Endpoint
Postoperative Discomfort
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

Inguinal hernia repair is one of the most commonly performed surgeries around the world. It accounts for approximately 75% of all abdominal wall hernias and presents a lifetime risk of 27% in males and 3% in females. Since the modern concept of surgical hernia repair described by Bassini in 1887, with the technique that bears his name, several techniques have been developed in the last century in order to improve surgical outcomes after inguinal hernia repair.

Different open repairs, such as anterior (Shouldice, McVay) or posterior (Stoppa) approach were described and developed, until Lichtenstein described the tension-free hernioplasty concept supported by the use of a prosthetic mesh to repair the hernia defect. Notable Improvements were observed with this technique in terms of recurrence, pain, and discomfort in comparison with previous tension repairs. Considerable advantages over open repair have been obtained with the introduction of minimally invasive surgery to inguinal hernia repair, in terms of patient comfort and recurrence rates.

Regarding prosthetic material, meshes have evolved since the first Dacron mesh used by Lichtenstein. First generation meshes were manufactured using more material and for this reason they have been described as heavyweight meshes. New generation meshes have been designed with less material in order to diminish the inflammatory response and foreign body reaction, providing less chronic pain with similar recurrence rates than heavyweight meshes. The density (or weight) of the mesh, measured in g/m2, is inversely proportional to the size of the pore and lately it has been reported that one of the main aspects related to prosthetic materials is pore size. Large pore meshes use less material, consequently they have been associated with a better tissue ingrowth. The large pore of lightweight meshes is conditioned by the less amount of material used.

All previous studies compare both light and heavyweight polypropylene meshes But in order to get a proper comparison of the behavior of meshes in the inguinal region it is important to include the material and the pore size. The aim of our study is to compare patient-reported outcomes with the use of either a Polytetrafluoroethylene (PTFE) large pore mesh (LP-PTFE) vs a small pore polypropylene mesh (SP-PPL).

Detailed Description

Patients fitted for laparoscopic bilateral inguinal hernia repair will be randomized to recieve one of both meshes on study in both inguinal sides.

Registry
clinicaltrials.gov
Start Date
January 2011
End Date
August 2013
Last Updated
12 years ago
Study Type
Interventional
Study Design
Crossover
Sex
Male

Investigators

Sponsor
Hospitales Universitarios Virgen del Rocío
Responsible Party
Principal Investigator
Principal Investigator

Salvador Morales Conde

Innovation and Minimally Invasive Surgery Unit Cordinator

Hospitales Universitarios Virgen del Rocío

Eligibility Criteria

Inclusion Criteria

  • male patients
  • 20-80 years old
  • Primary Bilateral Hernia

Exclusion Criteria

  • Recurrent hernias
  • Previous infraumbilical laparotomy
  • Inguinoscrotal hernias

Outcomes

Primary Outcomes

Postoperative Discomfort

Time Frame: 1 year

Postoperative Discomfort in the inguinal area is assessed using a visual analog scale (VAS)on the first 12 postoperative months. Discomfort is defined as a disturbing sensation without influencing normal activities of the patient

Secondary Outcomes

  • Postoperative Pain(1 year)
  • Recurrence(1 year)
  • Postoperative complications(1 year)

Study Sites (1)

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