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Aortic Aneurysm, Thoracic clinical trials

View clinical trials related to Aortic Aneurysm, Thoracic.

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NCT ID: NCT02777593 Active, not recruiting - Clinical trials for Aortic Aneurysm, Thoracic

Evaluation of the GORE® TBE Device in the Treatment of Lesions of the Aortic Arch and Descending Thoracic Aorta, Zone 2

SSB 11-02
Start date: September 6, 2016
Phase: N/A
Study type: Interventional

The objective of this study is to determine whether the GORE® TAG® Thoracic Branch Endoprosthesis is safe and effective in treating lesions of the aortic arch and descending thoracic aorta, requiring Zone 2 proximal implantation of the device.

NCT ID: NCT02777528 Active, not recruiting - Clinical trials for Aortic Aneurysm, Thoracic

Evaluation of the GORE® TAG® Thoracic Branch Endoprosthesis (TBE Device) in the Treatment of Lesions of the Aortic Arch and Descending Thoracic Aorta (Zone 0/1)

SSB 11-02
Start date: August 2016
Phase: N/A
Study type: Interventional

The objective of this study is to determine whether the GORE® TAG® Thoracic Branch Endoprosthesis is safe and effective in treating lesions of the aortic arch and descending thoracic aorta.

NCT ID: NCT02365467 Active, not recruiting - Clinical trials for Aortic Aneurysm, Thoracic, Chronic Type B Dissection

Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Descending TAA and Chronic Dissections

Start date: April 16, 2015
Phase:
Study type: Interventional

The purpose of the Feasibility study is to characterize the safety of the Valiant Mona LSA Thoracic Stent Graft System, including an assessment of the safety and effectiveness of the device acutely and at the 30 day visit in the identified subject population. This study will also evaluate the current instructions for use and may direct changes to the delivery and deployment steps. The purpose of the expansion to the Feasibility Study is to characterize the Valiant Mona LSA Thoracic Stent Graft System, in particular to assess the safety and effectiveness of the device acutely and at the 30 day visit, in subjects enrolled with chronic, Type B dissections.

NCT ID: NCT02294435 Active, not recruiting - Clinical trials for Thoracoabdominal Aneurysms

Visceral Manifold and Unitary Device Study for the Repair of Thoracoabdominal Aortic Aneurysms

Start date: February 2015
Phase: N/A
Study type: Interventional

The primary objective of the Visceral Manifold and Unitary Device Study is to assess the use of the thoracic bifurcation and the visceral manifold or the unitary device to repair thoracoabdominal aortic aneurysms in patients having appropriate anatomy. The primary intent of the study is to assess safety and preliminary effectiveness of the device. Additionally, the study will assess technical success and treatment success at each follow-up interval.

NCT ID: NCT01033214 Active, not recruiting - Clinical trials for Thoracic Aortic Aneurysm

ENTRUST - TAArget® Thoracic Stent Graft Clinical Trial

Start date: January 2010
Phase: Phase 1
Study type: Interventional

Evaluate the safety and effectiveness of endovascular repair with the LeMaitre TAArget thoracic stent graft as an alternative to open surgical repair.