To Assess the Predictive Value of D-dimer Level on the Occurrence of Cardiovascular Events (COAGFAII)

This study has been completed.
Sponsor:
Collaborator:
Ministry of Health, France
Information provided by:
Hopital Lariboisière
ClinicalTrials.gov Identifier:
NCT01224574
First received: September 13, 2010
Last updated: October 19, 2010
Last verified: September 2010

September 13, 2010
October 19, 2010
January 2001
July 2006   (final data collection date for primary outcome measure)
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Not Provided
Complete list of historical versions of study NCT01224574 on ClinicalTrials.gov Archive Site
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To Assess the Predictive Value of D-dimer Level on the Occurrence of Cardiovascular Events
Place Des D-dimères Dans la Prise en Charge Des Patients en Fibrillation Auriculaire : Evaluation de la Valeur prédictive Des D-dimères Sur la Survenue d'événements Thromboemboliques

The primary aim of the study was to assess whether D-Dimer level at entry or an increase of D-Dimer level during the follow-up could predict the occurrence of subsequent cardiovascular events in patients with atrial fibrillation.

Patients will be followed-up every 4 months with clinical assessment and D-dimer blinded measurement.

Observational
Observational Model: Cohort
Time Perspective: Prospective
Not Provided
Retention:   Samples Without DNA
Description:

No biospecimens are to be retained

Non-Probability Sample

Patients with atrial fibrillation encountered in usual care

Atrial Fibrillation
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Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
425
July 2007
July 2006   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • atrial fibrillation

Exclusion Criteria:

  • follow-up not possible, poor prognosis within 3 months
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
France
 
NCT01224574
AOR 01 029
No
Projet Hospitalier de Recherche Clinique Régional, Direction de la Recherche Clinique
Hopital Lariboisière
Ministry of Health, France
Principal Investigator: Isabelle Mahé, MD,PhD Hopital Lariboisière
Hopital Lariboisière
September 2010

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP