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DISSECT-N is an Observational Registry to Assess Real-world Safety and Effectiveness of the Valiant Navion Thoracic Stent Graft in Routine Clinical Practice in Subjects Diagnosed With a Dissection of the Thoracic Aorta

DISSECT-N is an Observational Registry to Assess Real-world Safety and Effectiveness of the Valiant Navion Thoracic Stent Graft in Routine Clinical Practice in Subjects Diagnosed With a Dissection of the Thoracic Aorta
Recruiting
18 years - 99 years
All
Phase N/A
30 participants needed
1 Location

Brief description of study

This is a prospective, observational, global, multi-center, post-market registry intended to assess the real-world safety and effectiveness of the Valiant Navion Stent Graft System in the treatment of thoracic aortic dissections. The primary objective is composite safety and effectiveness at 1-month post-procedure.

Eligibility of study

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

  • Conditions: Thoracic Aorta Dissection
  • Age: 18 years - 99 years
  • Gender: All

Male or Female, Age 18 or older, Subject was treated in the last 7 days, or is intended to be treated, with the Valiant Navion Thoracic Stent Graft System for a dissection in the thoracic aorta.

Updated on 04 Aug 2024. Study ID: 843475

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