Visceral Manifold Study for the repair of thoracoabdominal aortic aneurysms

Brief description of study

The purpose of this study is to evaluate the use of an investigational device called the ValiantTM Visceral Manifold Thoracoabdominal Stent Graft System for the repair of thoracoabdominal aortic aneurysms (TAAA), which is a balloon-like bulge in the aorta (major artery leading away from your heart) that originates in your chest and extends to your abdomen and also includes the branch arteries that supply blood to the liver, spleen, intestine, kidneys and other organs in your abdomen. The word investigational means the device is still being tested and is not approved by the Food and Drug Administration (FDA) for sale in the United States. The Visceral Manifold System is comprised of the Thoracic Bifurcation and Visceral Manifold to treat a thoracoabdominal aortic aneurysm or TAAA. Your aneurysm may or may not have a dissection.


Clinical Study Identifier: s16-01441
ClinicalTrials.gov Identifier: NCT03246126
Principal Investigator: Thomas Maldonado.
Other Investigator: Patrick J Lamparello.


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.