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Study of Surgical Mesh for Inguinal Hernia Repair

NCT00924755 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 25

Last updated 2010-10-04

No results posted yet for this study

Summary

The purpose of this study is to assess the early outcomes when using the Biomerix Revive™ as a tension-free onlay patch, Lichtenstein-style, in patients who are candidates for primary, unilateral, open inguinal hernia repair.

Conditions

  • Hernia, Inguinal

Interventions

DEVICE

Biomerix Revive™ (surgical mesh for inguinal hernia repair)

Inguinal hernia repair using a tension-free onlay patch, Lichtenstein-style.

Sponsors & Collaborators

  • Biomerix

    lead INDUSTRY

Principal Investigators

  • Samir S Awad, MD · Baylor College of Medicine

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
19 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-06-30
Primary Completion
2010-10-31
Completion
2010-11-30

Countries

  • United States

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 NCT00924755 on ClinicalTrials.gov