Observatory of Screening Aneurysms of the Abdominal Aorta During Echocardiography. National Epidemiological Survey (E2T3A)
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|ClinicalTrials.gov Identifier: NCT01390740|
Recruitment Status : Completed
First Posted : July 11, 2011
Last Update Posted : November 24, 2017
Study of the prevalence of Abdominal Aortic Aneurysms (AAA) (> 3 cm) in patients with echocardiography (transthoracic or) during a specific day, with cardiologists in France.
This is a cross-sectional epidemiological investigation, assembling evidence from a routine ultrasound screening for AAA at the waning of echocardiograms performed during a specific day.
The study will be offered a list of centers selected by the Scientific Committee in the complete list of locations being in France, the subsidiary of echocardiography Echocardiography of French Society of Cardiology. These centers will be 500 in number representative of the French centers, geographically and by type of centers.
|Condition or disease|
|Abdominal Aortic Aneurysms|
Multicenter observational study collecting data from a routine ultrasound screening for AAA at the waning of echocardiograms performed during a specific day. All of the cardiologists practicing echocardiography are invited to participate in this study, each cardiologist should include echocardiography in 10 patients examined for any reason and will be considered referring cardiologist.
There will be no follow-up, the idea is to have a database with measures of abdominal aortic aneurysms and therefore.
|Study Type :||Observational|
|Actual Enrollment :||1412 participants|
|Official Title:||Observatory of Screening Aneurysms of the Abdominal Aorta During Echocardiography. National Epidemiological Survey|
|Study Start Date :||May 2011|
|Actual Primary Completion Date :||September 2011|
|Actual Study Completion Date :||September 2011|
patients with echocardiography
- Prevalence of patients with AAA among those with echocardiography. [ Time Frame: 1 day ]Discovery of the aneurysm of the abdominal aorta at the waning of echocardiography
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01390740
|Office of Cardiology Kownator|