RECRUITING

Post-market Study of the Biodesign Hernia Graft

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

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.

Official Title

Post-market Study of the Biodesign® Hernia Graft

Quick Facts

Study Start:2020-11-10
Study Completion:2027-06-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04294446

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.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Primary or recurrent ventral hernia in need of surgical repair utilizing a Biodesign Hernia Graft
  1. 1. Known sensitivity to porcine material
  2. 2. Age \< 18 years
  3. 3. Unable or unwilling to provide informed consent
  4. 4. Life expectancy of less than one year from the date of the index procedure
  5. 5. Patients will be excluded from the study if they never receive a Biodesign Hernia Graft during their index procedure.

Contacts and Locations

Study Contact

Samantha Stevenson, BS
CONTACT
765-497-3385
sstevenson@rtix.com
Jason Hodde, MS
CONTACT
765-497-3385
jhodde@rtix.com

Study Locations (Sites)

Vanderbilt University Medical Center
Nashville, Tennessee, 37232
United States

Collaborators and Investigators

Sponsor: Cook Biotech Incorporated

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2020-11-10
Study Completion Date2027-06-30

Study Record Updates

Study Start Date2020-11-10
Study Completion Date2027-06-30

Terms related to this study

Additional Relevant MeSH Terms

  • Ventral Hernia