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Enrolling By Invitation
99 years or below
All
Phase N/A
1 Location

Brief description of study

This is a prospective, multi-center, non-randomized, single arm, post-market study designed to evaluate the Thoraflex Hybrid device alone and in combination with the RelayPro NBS stent-graft in the treatment of aortic disease affecting the aortic arch and descending aorta with or without involvement of the ascending aorta.

Eligibility of study

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

  • Conditions: Medical Research
  • Age: 99 years or below
  • Gender: All

TBD

Updated on 16 Dec 2024. Study ID: 23-0066
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Study is selecting its participants from a population, or group of people, decided on by the researchers in advance.

Contact Office of Clinical Research