COPART - Longitudinal Study on Patients Hospitalised for Artery Disease

Head :
Bura-Riviere Alessandra, U1048 Institut des maladies métaboliques et cardiovasculaires (I2MC)Équipe/activité : Production et fonction plaquettaire, signalisation et phosphoinositides

Last update : 08/05/2015 | Version : 2 | ID : 8949

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Métadonnées
Identification
General Aspects
Scientific investigator(s) (Contact)
Collaborations
Funding
Governance of the database
Additional contact
Type of database
Database objective
Population type
Dates
Size of the database
Data
Procedures
Promotion
Access
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General
Identification
Detailed name Longitudinal Study on Patients Hospitalised for Artery Disease
Sign or acronym COPART
General Aspects
Medical area Cardiology
Health determinants Genetic
Keywords systolic pressure index, coronary and cerebrovascular events, hospitalisation
Scientific investigator(s) (Contact)
Name of the director Bura-Riviere
Surname Alessandra
Address 1 av du professeur Jean Poulhes BP 84225 31432 Toulouse CEDEX 4
Phone +33 (0)5 61 32 27 05
Email bura-riviere.a@chu-toulouse.fr
Unit U1048 Institut des maladies métaboliques et cardiovasculaires (I2MC)Équipe/activité : Production et fonction plaquettaire, signalisation et phosphoinositides
Organization CHU Toulouse ;
Collaborations
Funding
Funding status Public
Details CHU
Governance of the database
Sponsor(s) or organisation(s) responsible CHU Toulouse
Organisation status Public
Sponsor(s) or organisation(s) responsible Institut national de la santé et de la recherche médicale - Inserm
Organisation status Public
Additional contact
Main features
Type of database
Type of database Study databases
Study databases (details) Longitudinal study (except cohorts)
Database recruitment is carried out by an intermediary A selection of health institutions and services
Database recruitment is carried out as part of an interventional study No
Additional information regarding sample selection. All patients with peripheral artery disease that were hospitalised in the vascular medicine department of the Rangueil university hospital between 01/06/2004 and 31/07/2006 were consecutively included.
Database objective
Main objective To form a database on peripheral artery disease of the lower limbs in hospitalised patients that is atheromatous in origin, which shall allow the treatment, monitoring and prognosis of affected patients to be assessed. This study aims to compare prescribed treatment upon discharge from hospital and French National Health Authority recommendations and to evaluate the trends in prescribed treatment over time.
Inclusion criteria - male and female
- adult
- patients with peripheral artery disease hospitalised in the vascular medicine department
Patients that died during hospitalisation were excluded from the study.
Population type
Age Adulthood (45 to 64 years)
Elderly (65 to 79 years)
Great age (80 years and more)
Population covered Sick population
Gender Male
Woman
Geography area Local
French regions covered by the database Aquitaine Limousin Poitou-Charentes
Languedoc-Roussillon Midi-Pyrénées
Detail of the geography area Toulouse
Data collection
Dates
Date of first collection (YYYY or MM/YYYY) 06/2004
Date of last collection (YYYY or MM/YYYY) 06/2005
Size of the database
Size of the database (number of individuals) < 500 individuals
Details of the number of individuals 400
Data
Database activity Current data collection
Type of data collected Declarative data
Paraclinical data
Administrative data
Declarative data (detail) Paper self-questionnaire
Paraclinical data (detail) Restenosis or bypass obstruction diagnosis will be by ultrasound or imaging.
Administrative data (detail) Information on the patient's vital status will be requested from the town/city hall where the patient was born or residing. This is applicable for all patients.
Presence of a biobank No
Health parameters studied Health event/morbidity
Health event/mortality
Health care consumption and services
Care consumption (detail) Hospitalization
Medical/paramedical consultation
Procedures
Participant monitoring Yes
Details on monitoring of participants Follow-up is annual. Each patient should have information regarding their outcome at one year. Events that occurred during follow-up will be listed
Links to administrative sources No
Promotion and access
Promotion
Link to the document http://www.portailvasculaire.fr/espace-sfmv/etude-copart
Link to the document http://tinyurl.com/Hal-COPART
Description List of publications in HAL
Link to the document http://www.ncbi.nlm.nih.gov/pubmed/?term=copart
Description List of publications in Pubmed
Access
Terms of data access (charter for data provision, format of data, availability delay) Contact the scientist in charge.
Access to aggregated data Access on specific project only
Access to individual data Access on specific project only

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