ACTIVE_NOT_RECRUITING

Assessment of GORE® SYNECOR Biomaterial in Focused Patient Populations and Long-Term Application

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Conditions

Hernia, VentralHernia IncisionalHernia Incisional VentralHernia RepairHernia Mesh TreatmentVentral HerniaIncisional HerniaIntraperitonealPreperitoneal

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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 SYN 20-01 Study is a non-interventional, prospective, multicenter, multicohort, international, post-market clinical investigation looking into the assessment of GORE® SYNECOR Biomaterial in focused patient populations and in long-term application. Patients with ventral / incisional hernia amenable to hernia mesh repair will be enrolled into two cohorts (US and EU cohort) and followed-up over the period of 60 months.

Official Title

Assessment of GORE® SYNECOR Biomaterial in Focused Patient Populations and Long-Term Application

Quick Facts

Study Start:2023-02-24
Study Completion:2030-07-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT05094089

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 to 80 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Locations (Sites)

Emory Saint Joseph's Hospital
Atlanta, Georgia, 30342
United States
Tufts Medical Center
Boston, Massachusetts, 02111
United States
Corewell Health
Grand Rapids, Michigan, 49506
United States
Lovelace Women's Hospital
Albuquerque, New Mexico, 87109
United States
Stony Brook University Hospital
Stony Brook, New York, 11794
United States
Novant Health New Hanover Regional Medical Center
Wilmington, North Carolina, 28401
United States
Prisma Health Greenville Memorial Hospital
Greenville, South Carolina, 29605
United States
Bon Secours Memorial Regional Medical Center
Mechanicsville, Virginia, 23116
United States

Collaborators and Investigators

Sponsor: W.L.Gore & Associates

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 Date2023-02-24
Study Completion Date2030-07-31

Study Record Updates

Study Start Date2023-02-24
Study Completion Date2030-07-31

Terms related to this study

Keywords Provided by Researchers

  • Hernia Repair
  • Hernia Mesh Treatment
  • Ventral Hernia
  • Incisional Hernia
  • Intraperitoneal
  • Preperitoneal

Additional Relevant MeSH Terms

  • Hernia, Ventral
  • Hernia Incisional
  • Hernia Incisional Ventral