Status and phase
Conditions
Treatments
About
The objective of this study is to assess the safety and effectiveness of the Cordis Bilateral AAA device and its Delivery System compared to open surgical repair for the treatment of Abdominal Aortic Aneurysm (AAA).
Sex
Ages
Volunteers
Inclusion criteria
Aortic Aneurysm Diameter
Aortic Neck
Angulation Neck Length < 45° > 15 mm <60° > 25 mm
Iliac Arteries
Diameter Aortic Neck Common Iliac 26-28 mm 13-18 mm 23-25.9 mm 10-17 mm 20-22.9 mm 9-15 mm 17-19.9 mm 8-13 mm 14-16.9 mm 8-11mm
*NOTE: An aortic diameter cannot be treated if the iliac diameter is not in the same range (e.g. 26-28 mm aortic necks must be in conjunction with 13-18 mm common iliacs).
Anatomic (surgical controls)
· Surgical controls will be required to meet only the aortic or aorto-iliac aneurysm size requirements for anatomic inclusion criteria.
Aortic Aneurysm Diameter
Surgical control patients will be required to meet all of the above-stated stent-graft clinical inclusion criteria.
Exclusion criteria
Anatomic (stent-graft)
Aortic Aneurysm Diameter
· < 4.5 cm that are not at least 1.5 times the diameter of the aorta with evidence of a size increase of 5 mm or greater within a six month period.
Aorto-iliac Aneurysms
Aortic Neck
Diameter < 17 mm and > 28 mm (Phase I)
Diameter < 14 and >28 (Phase II)
Thrombus lined
Highly calcified
Iliac Arteries
< 8 mm and > 18 mm (native) (Phase I and Phase II)
Highly calcified (common)
Neither common iliac artery with a cuff > 15 mm.
Anatomic (surgical controls)
· Surgical controls will be excluded based only on the aortic or aorto-iliac aneurysm size requirements for anatomic exclusion criteria.
Aortic Aneurysm Diameter
· < 4.5 cm that are not at least 1.5 times the diameter of the aorta with evidence of a size increase of 5 mm or greater within a six month period.
Aorto-Iliac Aneurysms
Clinical (stent-graft)
Primary purpose
Allocation
Interventional model
Masking
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Data sourced from clinicaltrials.gov
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