Absorbable Sutures , Non Absorbable Sutures or Biologic Fibrin Glue for Protesic Mesh Fixing in Lichtenstein Technique for Primitive Groin Hernia Repair: a Randomized Prospective Multicentric Trial

NCT02011698 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 900

Last updated 2013-12-13

No results posted yet for this study

Summary

this study has the aim to analize the correlation between three different methods of mesh fixation ( using absorbable or non absorbable sutures or fibrin biological glue) and recurrance and chronic pain ,in the Lichtenstein anterior inguinal erniorrhaphy

Conditions

  • Hernia, Inguinal

Interventions

PROCEDURE

Lichtenstein technique groin hernia repair with mesh. Use of absorbale sutures for mesh fixation

PROCEDURE

Lichtenstein technique groin hernia repair with mesh. Use of non absorbable sutures for mesh fixation

PROCEDURE

Lichtenstein technique groin hernia repair with mesh. Use of fibrin biological glue for mesh fixation

Sponsors & Collaborators

  • Ospedale di Circolo - Fondazione Macchi

    lead OTHER

Principal Investigators

  • Lorenzo Latham, MD · Department of Surgery. Azienda Ospedaliera Ospedale di Circolo e Fondazione Macchi

  • Eugenio Cocozza, MD · Department of Surgery. Azienda Ospedaliera Ospedale di Circolo e Fondazione Macchi

  • Lorenzo Livraghi, MD · Department of Surgery. Azienda Ospedaliera Ospedale di Circolo e Fondazione Macchi

  • Mattia Berselli, MD · Department of Surgery. Azienda Ospedaliera Ospedale di Circolo e Fondazione Macchi

  • Bianca Gambitta, Student · Department of Surgery. Azienda Ospedaliera Ospedale di Circolo e Fondazione Macchi

  • Luca Farassino, MD · Department of Surgery. Azienda Ospedaliera Ospedale di Circolo e Fondazione Macchi

  • Ildo Scandroglio, MD · Department of surgery Azienda Ospedaliera di Busto Arsizio Ospedale di Tradate

  • Francesco Roscio, MD · Department of surgery Azienda Ospedaliera di Busto Arsizio ospedale di Tradate

  • Dario Maggioni, MD · Azienda Ospedaliera, Ospedale Civile di Legnano

  • Angelo Miranda, MD · Azienda Ospedaliera, Ospedale Civile di Legnano

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-10-31
Primary Completion
2015-10-31
Completion
2016-10-31

Countries

  • Italy

Study Locations

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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 NCT02011698 on ClinicalTrials.gov