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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT00445835 |
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Date of registration:
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08/03/2007 |
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Primary sponsor: |
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Public title:
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Active Detection of the Extension of Atherothrombosis in High Risk Coronary Patients
AMERICA |
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Scientific title:
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Active Detection and Management of the Extension of Atherothrombosis in High Risk Coronary Patients In Comparison With Standard of Care for Coronary Atherosclerosis: The AMERICA Study |
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Date of first enrolment:
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September 2007 |
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Target sample size:
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526 |
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Recruitment status: |
Active, not recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT00445835 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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Countries of recruitment
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France
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Contacts
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Name:
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Jean-Philippe COLLET, MD PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Assistance Publique - Hôpitaux de Paris |
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Key inclusion & exclusion criteria
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Inclusion criteria:
1. Three vessel disease recently identified recently (<6 month)
2. Accrue coronary syndromes in patients>75 years old (<1 month)
Exclusion criteria:
1. Absence of significant coronary lesions
2. Other causes of rise in the troponin level
3. Patient<18 years old
4. Pregnant women
5. Patient without affiliation to National Social Security
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Coronary Artery Disease
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Intervention(s)
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Other: Arterial doppler for screening asymptomatic and significant extracoronary arterial stenoses in all arterial beds
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Other: Conservative arm
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Primary Outcome(s)
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death (all cause) or any ischemic event leading to rehospitalisation or any evidence of organ failure.
[Time Frame: during the study]
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Secondary Outcome(s)
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Incidence of each composite of the primary endpoint.
[Time Frame: during the study]
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Secondary ID(s)
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P060902
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PHAO 2006
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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