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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00299624
Other study ID # TAPH
Secondary ID
Status Completed
Phase N/A
First received March 6, 2006
Last updated September 13, 2010
Start date October 2005
Est. completion date August 2006

Study information

Verified date September 2010
Source Hopital Lariboisière
Contact n/a
Is FDA regulated No
Health authority France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Study type Observational

Clinical Trial Summary

Aging is an independent risk factor, without any clear explanation. The primary aim of the study is to depict the effect of aging on the coagulation fibrinolysis parameters and microparticles.


Description:

Patients older than 40, without any acute disease and not receiving any antiaggregant and anticoagulant therapy will be included in the study. Blood tests will be performed for coagulation, fibrinolysis and microparticles measurement.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date August 2006
Est. primary completion date August 2006
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 40 Years and older
Eligibility Inclusion Criteria:

- age <40 2 groups : 1 : no history of VTE 2 : history of VTE

Exclusion Criteria:

- antiaggregant or anticoagulant therapy at curative dose

- arterial or thrombotic event in the last month

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
France Hopital Lariboisiere Paris
France Hopital Lariboisière Paris

Sponsors (1)

Lead Sponsor Collaborator
Hopital Lariboisière

Country where clinical trial is conducted

France, 

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