Registry for Patients Receiving an Endovascular Device made by GORE

What we are studying

This is a registry for GORE collecting data from patients that receive a GORE endovascular device. The devices being used have been approved by the FDA and are commercially available.

Who we are studying

  • Men and Women
  • Races:
    • White
    • African American
    • Asian
    • American Indian or Alaska Native
    • Native Hawaiian or Pacific Islander
    • Other
  • Not Hispanic or Latino
  • Ages 18+

Eligibility Criteria

  • Any subject receiving an Endovascular GORE device

What is involved

  • This is only a collection of data from any procedure using any endovascular GORE device and any follow up visits thereafter

Compensation

None

Contact Information

Study Coordinator
Rob Paris
Email
rparis@wakehealth.edu
Phone
336-716-3296
Principal Investigator
Matthew Corriere, M.D.

Disclaimer: The information on this website is for general informational purposes only and SHOULD NOT be relied upon as a substitute for sound professional medical advice, evaluation or care from your physician or other qualified health care provider.