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Efficacy Study of Tissucol/Tisseel Fibrin Sealant to Treat Inguinal Hernia

NCT00306839 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 325

Last updated 2009-02-13

No results posted yet for this study

Summary

The purpose of the study is to evaluate mid and long term postoperative pain and further disabling complications in open inguinal hernia repair by Lichtenstein technique after mesh fixation with fibrin sealant (FS), compared to mesh fixation with sutures.

Conditions

  • Inguinal Hernia

Interventions

PROCEDURE

standardized Lichtenstein technique

Sponsors & Collaborators

  • Baxter Healthcare Corporation

    collaborator INDUSTRY

  • Pr Giampiero CAMPANELLI

    collaborator UNKNOWN

  • University of Milan

    lead OTHER

Principal Investigators

  • CAMPANELLI Giampiero, Professor

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-02-28
Completion
2008-05-31

Countries

  • Belgium
  • Denmark
  • France
  • Germany
  • Spain
  • United Kingdom

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 NCT00306839 on ClinicalTrials.gov