Post-market Study of the Biodesign Hernia Graft

Description

The purpose of this study is to collect data on the performance of the Biodesign® Hernia Graft when used to reinforce soft tissues during ventral hernia repair.

Conditions

Ventral Hernia

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Study Overview

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Study Details

Study overview

The purpose of this study is to collect data on the performance of the Biodesign® Hernia Graft when used to reinforce soft tissues during ventral hernia repair.

Post-market Study of the Biodesign® Hernia Graft

Post-market Study of the Biodesign Hernia Graft

Condition
Ventral Hernia
Intervention / Treatment

-

Contacts and Locations

Nashville

Vanderbilt University Medical Center, Nashville, Tennessee, United States, 37232

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Primary or recurrent ventral hernia in need of surgical repair utilizing a Biodesign Hernia Graft
  • 1. Known sensitivity to porcine material
  • 2. Age \< 18 years
  • 3. Unable or unwilling to provide informed consent
  • 4. Life expectancy of less than one year from the date of the index procedure
  • 5. Patients will be excluded from the study if they never receive a Biodesign Hernia Graft during their index procedure.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Cook Biotech Incorporated,

Study Record Dates

2027-06-30