Safety and Efficacy of Valiant Mona LSA Stent Graft System
Status: | Completed |
---|---|
Conditions: | Cardiology, Cardiology |
Therapuetic Areas: | Cardiology / Vascular Diseases |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 2/17/2019 |
Start Date: | April 2013 |
End Date: | December 2018 |
Valiant Mona LSA Stent Graft System Early Feasibility Study
The Valiant Mona LSA thoracic stent graft system is for the endovascular repair of aneurysms
of the descending thoracic aorta (DTA) in patients who require coverage of the left
subclavian artery (LSA).The study is intended to assess safety and performance of the device
acutely and at 30 days.
of the descending thoracic aorta (DTA) in patients who require coverage of the left
subclavian artery (LSA).The study is intended to assess safety and performance of the device
acutely and at 30 days.
Inclusion Criteria:
- Subject is at least 18 years of age.
- The subject or legal guardian understands the nature of the study and agrees to its
provisions on a written informed consent form
- Subject must be considered a candidate for revascularization of the LSA.
- Subject has a DTA which will require coverage of the LSA
- Subject's anatomy must meet the anatomical criteria to receive that implanted device
Exclusion Criteria:
- Subject has had previous endovascular repair of the ascending and/or descending
thoracic aorta.
- Subject is in acute renal failure or has renal insufficiency with a serum creatinine ≥
2.0 mg/dL
- Subject is a pregnant female.
- Enrollment in another clinical study
- Subject has had a cerebral vascular accident (CVA)or myocardial infarction (MI) within
3 months.
- Subject has a history of bleeding diathesis, coagulopathy, or refuses blood
transfusion.
- Subject has a known allergy or intolerance to the device components.
- Subject has a known hypersensitivity or contraindication to anticoagulants or contrast
media, which is not amenable to pre-treatment.
We found this trial at
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