Aortic dissection: Research Studies

Be an Informed Participant

Before deciding to participate in a research study, take time to learn about clinical research, how it's conducted and your rights as a research participant. Following are some helpful resources from independent sources. Always remember that a clinical research study is research, not treatment.

Know Who to Contact

  • Eligibility: For questions about a specific study and who is eligible to participate, call or email the contact person listed for that study.
  • Your Rights: For questions about your rights as a research participant, contact the UF Institutional Review Boards at 352-273-9600.
  • Feedback: For general questions or feedback about study listings, email the UF Clinical and Translational Science Institute at UFStudies@health.ufl.edu.

Other Resources

  • ResearchMatch.org: Join a national registry of volunteers willing to be contacted about research studies.

For Research Teams

4 Related Result(s)

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  1. Zenith Dissection Endovascular System in the Treatment of Patients with Aortic Dissections

    The purpose is to study the safety and effectiveness of the Zenith Dissection Endovascular System in the treatment of acute, complicated Type B aortic...

  2. Study of the RelayPro Thoracic Stent-Graft in Subjects With an Acute, Complicated Type B Aortic Dissection

    A study is recruiting adults 18 years and older with acute, complicated type B aortic dissection. For study details, please contact the UF Health...

  3. Zenith Dissection Endovascular System in the Treatment of Patients With Aortic Dissections

    The Zenith Dissection extended...

  4. Evaluation of the GORE® TAG® Thoracic Branch Endoprosthesis (TBE Device) in the Treatment of Lesions of the Aortic Arch and Descending Thoracic Aorta (Zone 2) (SSB 11-02)

    Composite of the following events through one month: initiation of the index endovascular procedure following the debranching procedure, device technical...

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Studies listed on this site have been approved by a UF Institutional Review Board (IRB), which works to ensure the welfare and rights of research participants as required by federal regulations. Study listings are provided by the UF Clinical and Translational Science Institute in collaboration with UF research teams and the UF IRBs.