4 studies in Aortic Aneurysm
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Zenith(R) Low Profile AAA Endovascular Graft Clinical Study
Rochester, MN
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Zenith(R) Low Profile AAA Endovascular Graft Clinical Study
Location:
Rochester, MNTrial status:
Open for EnrollmentWhy is this study being done?
The Zenith(R) Low Profile AAA Endovascular Graft Clinical Study is a clinical trial approved by US FDA to study the safety and effectiveness of the Zenith(R) Low Profile AAA Endovascular Graft in the treatment of abdominal aortic, aorto-iliac, and iliac aneurysms.
NCT ID:
NCT00833924Who can I contact for additional information about this study?
Rochester: Gustavo Oderich, MD 507-255-7208
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TX2® Low Profile TAA Endovascular Graft
Rochester, MN
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TX2® Low Profile TAA Endovascular Graft
Location:
Rochester, MNTrial status:
Open for EnrollmentWhy is this study being done?
The Zenith® TX2® Low Profile TAA Endovascular Graft study is a clinical trial approved by US FDA to evaluate the safety and effectiveness of the Zenith® TX2® Low Profile TAA Endovascular Graft indicated for the treatment of patients with aneurysms/ulcers of the descending thoracic aorta having vessel structure suitable for repair.
NCT ID:
NCT01151020Who can I contact for additional information about this study?
Rochester: Gustavo Oderich, MD 507-225-7208
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Hydrogel Endovascular Aneurysm Treatment Trial
Jacksonville, FL
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Hydrogel Endovascular Aneurysm Treatment Trial
Location:
Jacksonville, FLTrial status:
Open for EnrollmentWhy is this study being done?
Your part in this study will last up to 24 months and will involve 6 visits (1 baseline visit before your surgery, the surgical procedure and 4 follow-up visits). These visits will occur at the same time as the visits you would receive as standard of care after your surgery. If you are in this study, you will be placed in one of two study groups by chance using a process similar to the flip of a coin. This process is called randomization. Neither you nor the study staff will select the group you will be in. One group, the control group, will have their aneurysm treated by the bare platinum coils during their endovascular procedure. The other group, the study group will receive coils from the HydroCoil Embolization System. Both groups will receive the same standard of care and follow-up, but during the surgery different types of coils will be used.
NCT ID:
NCT01407952Who can I contact for additional information about this study?
Jacksonville: Jessie Sperrazza 904-953-9494
Dale Gamble 904-953-9612
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Safety and Effectiveness Trial of the Ventana Fenestrated Stent Graft System
Rochester, MN
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Safety and Effectiveness Trial of the Ventana Fenestrated Stent Graft System
Location:
Rochester, MNTrial status:
Open for EnrollmentWhy is this study being done?
The purpose of this trial is to determine if the Ventana Fenestrated Stent Graft System is safe and effective for the endovascular repair of juxtarenal or pararenal aortic aneurysms.
NCT ID:
NCT01491945Who can I contact for additional information about this study?
Rochester: Sharon Mueller 507-538-0992

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