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Comparative Study of Inguinodynia After Inguinal Hernia Repair

NCT03678272 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 270

Last updated 2018-09-19

No results posted yet for this study

Summary

To evaluate the postoperative pain and the relapse after the repair of the inguinal hernia by Lichtenstein technique with four different mesh types with different types of fixation in patients undergoing major ambulatory surgery.

Conditions

  • Inguinal Hernia
  • Inguinal Hernia Repair
  • Open Inguinal Hernia

Interventions

PROCEDURE

HERNIOPLASTY WITH PANAVALE MESH

Polypropylene mesh fixed with 3 points. Preformed polypropylene mesh will be used by fixing it with one point to the pubis, another to the inguinal ligament and another to the joint tendon.

PROCEDURE

HERNIOPLASTY WITH PARIETEX PROGRIP MESH

Preformed polypropylene mesh will be used which presents a self adhesive system not based on glue, but on the arrangement of the fibers of the mesh as "hooks", and to which we will give a single point to the pubis.

PROCEDURE

HERNIOPLASTY WITH ADHESIX MESH

It will use a self-adhesive mesh without giving points to fix this one, since it is a mesh that integrates the glue.

PROCEDURE

HERNIOPLASTY WITH TIMESH MESH

Titaniumized polypropylene mesh will be used without fixing points, since liquid cyanoacrylate (Ifabond) will be used to fix it.

Sponsors & Collaborators

  • Hospital General Universitario Elche

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-04-30
Primary Completion
2015-03-31
Completion
2016-03-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03678272 on ClinicalTrials.gov