Cordis Bilateral AAA Device Compared to Open Surgical Repair of Abdominal Aortic Aneurysms (ARIBA)

Completed · Phase 1/Phase 2

Conditions studied: Abdominal Aortic Aneurysm

In brief

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).

Key facts

Study ID

NCT00235118

Run by

Cordis US Corp.

People needed

29

Starts

1999-12-01

Expected to finish

2006-02-01

Last updated by the study team

2005-12-09

Who can join

Age: 40 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Anatomic (stent-graft)
• Aortic Aneurysm Diameter
• > 4.5 cm
• Those aortic aneurysms < 4.5 cm that are at least 1.5 times the diameter of the aorta with a size increase of 5 mm or greater over a six month period will also be included for possible treatment.
• Aorto-iliac aneurysms in which the aortic aneurysm is < 4.5 cm but the iliac artery aneurysms are > 3.0 cm in diameter or there is evidence of recent expansion (5 mm or greater over a six month period) in iliac aneurysms < 3.0 cm.
• Saccular aortic aneurysms > 3.0 cm.
• Aortic Neck
• Diameter > 17 mm and < 28 mm (Phase I)
• Diameter > 14 mm and < 28 mm (Phase II)
• Angulation Neck Length < 45° > 15 mm <60° > 25 mm
• Iliac Arteries
• Diameter > 8 mm and < 18 mm (Phase I and Phase II)
• At least one common iliac artery with a cuff > 15 mm.
• 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
• > 4.5 cm
• Those aortic aneurysms <4.5 cm that are at least 1.5 times the diameter of the aorta with a size increase of 5 mm or greater over a six month period will also be included for possible treatment.
• Aorto-iliac aneurysm in which the aortic aneurysm is <4.5 cm but the iliac artery aneurysm are >3.0 cm in diameter or there is evidence of recent expansion (5 mm or greater over a six month period) in iliac aneurysms <3.0 cm.
• Saccular aortic aneurysms > 3.0 cm.
• Clinical (stent-graft)
• Males and non-pregnant females > 40 years of age.
• Clinical (surgical controls)

You may not qualify if…

• 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
• < 3.0 cm in diameter unless evidence of recent expansion (5 mm or greater within a six month period).
• The iliac portion of the aneurysm extending to the bifurcation bilaterally which would necessitate covering both internal iliac arteries with the device.
• Aortic Neck
• Diameter < 17 mm and > 28 mm (Phase I)
• Diameter < 14 and >28 (Phase II)
• Thrombus lined
• Highly calcified
• NOTE: See inclusion criteria for length below the renals and degree of angulation.
• 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.
• NOTE: See inclusion criteria for aortic neck and iliac artery diameters.
• 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
• < 3.0 cm in diameter unless evidence of recent expansion (5 mm or greater within a six month period).
• The iliac portion of the aneurysm extending to the bifurcation bilaterally which would necessitate surgically covering both internal iliac arteries.
• Clinical (stent-graft)

Where it is running

• Mt. Sinai Hospital — New York, New York, United States

Full record on ClinicalTrials.gov

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