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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00496717
Other study ID # 3914
Secondary ID
Status Completed
Phase N/A
First received July 3, 2007
Last updated July 27, 2011
Start date July 2007
Est. completion date December 2008

Study information

Verified date May 2011
Source University Hospital, Strasbourg, France
Contact n/a
Is FDA regulated No
Health authority France: Ministry of Health
Study type Observational

Clinical Trial Summary

Calcium scoring of the coronary arteries is use as a predictor of coronary stenosis. The aim of this study is to measure the calcium scoring of the abdominal aorta using an helicoidal fast scan and to correlate this measurement with classical cardiovascular risk factors and newer parameters reflecting vascular rigidity, like pulse velocity measurement.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date December 2008
Est. primary completion date December 2008
Accepts healthy volunteers No
Gender Both
Age group 45 Years and older
Eligibility Inclusion criteria :

- Patients with at least one cardiovascular risk factor

- Ambulatory or hospitalized patients

Exclusion criteria :

- Significant cardiovascular complications

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Device:
Helicoidal fast scann
Each patient will have an computed aortic tomodensitometric scan without contrast injection. This procedure lasts few minutes and irradiation is low. The aortic calcium scoring is calculated using a specific program included in the scan machine

Locations

Country Name City State
France Service d'Hypertension, Maladies Vasculaires et Pharmacologie Clinique, Nouvel Hôpital Civil, Hôpitaux Universitaires de Strasbourg Strasbourg
France Service de Radiologie, Hôpital Civil Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

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