The ELUTES Clinical Trial
Completed · Not applicable
Conditions studied: Coronary Artery Disease
In brief
ELUTES is a European multicenter, randomized, controlled, triple-blinded study designed to evaluate the ability of the Paclitaxel Eluting V-Flex Plus coronary stent to reduce restenosis in the coronary artery.
Key facts
- Study ID
- NCT00225654
- Run by
- Cook Group Incorporated
- People needed
- 192
- Starts
- 2000-01-01
- Expected to finish
- 2001-11-01
- Last updated by the study team
- 2012-02-01
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patient must be eligible to undergo planned treatment of a single de novo lesion in a native coronary artery.
- Patient must be an acceptable candidate for coronary artery bypass surgery.
- Patient or legal guardian must have signed informed consent.
- Patient agrees to return at one month for an office visit to assess cardiovascular status and at 6 months for an office visit to assess cardiovascular status and for a diagnostic angiogram.
You may not qualify if…
- Patient must be less than 18 years old.
- Patient has history of bleeding diathesis or coagulopathy or will refuse blood transfusions.
- Patient is simultaneously participating in another investigative interventional cardiovascular device or drug study.
- Patient has known hypersensitivity or contraindication to aspirin, clopidogrel, or stainless steel, or a sensitivity to contrast dye.
- Women of child bearing potential.
- Patient has other medical condition that may cause non-compliance with the protocol, confound the results, or is associated with limited life expectancy.
- Patient has been diagnosed with a myocardial infarction within 72 hours prior to procedure.
Where it is running
- Contact Sponsor — Bloomington, Indiana, United States
Full record on ClinicalTrials.gov
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