RelayPro Aneurysm trial

Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions:
    Thoracic Aneurysms And Penetrating Ulcers
  • Age: Between 18 - 100 Years
  • Gender: Male or Female
  • Other Inclusion Criteria:
    1. Subject must be at least 18 years of age
    2. Subject has specified disease in his/her descending thoracic aorta.
    3. Subject have anatomical compliance for the device specified for both access vessels and treatment area.
    4. Subject must be willing to comply with the follow-up evaluation schedule.
    5. Subject(or Legally Authorized Representative) agrees an Informed Consent Form prior to treatment.

You may not be eligible for this study if the following are true:

    1. Subject has specified disease of the thoracic aorta which is not included in the trial, for example: aortic dissection, intramural hematoma, traumatic injury or transection, aortic false aneurysm, ruptured aneurysm.
    2. Subject anatomy with significant stenosis, calcification, thrombus or tortuosity.
    3. Subjects with specified compromised circulation.
    4. Subjects with specified prior procedures.
    5. Subjects with allergy to contrast media or device components.
    6. Subjects with disease, for example: suspected connective tissue disorder, specified coagulation disorders, specified coronary artery disease, severe congestive heart failure, stroke and/or Myocardial Infarction (MI) as specified, specified pulmonary disease, specified renal failure.
    7. Subjects that are pregnant or planning to become pregnant during the course of the study.



If you are registered as a volunteer, please log in to contact the study team/express interest in this study.

Contact the research team to learn more about this study.

By clicking "Contact Research Team", your contact information will be sent securely to the research staff associated with the study. You will also receive a copy of this email in your inbox, as well as other notifications to determine your participation status in the study.