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Assessment of lipid-lowering treatment in France

Belgium, France, Greece...and 4 more, 2006
Reference ID
FRESH-PEF6396-en
Producer(s)
Jean Ferrières
Metadata
DDI/XML JSON
Created on
Nov 15, 2025
Last modified
Nov 15, 2025
Page views
4
  • Study Description
  • Get Microdata
  • Identification
  • Scope
  • Coverage
  • Producers and sponsors
  • Study authorization
  • Sampling
  • Survey instrument
  • Data collection
  • Study activities
  • Data Access
  • Contacts
  • Metadata production
  • Identification

    Survey ID number

    FRESH-PEF6396-en

    Title

    Assessment of lipid-lowering treatment in France

    Abbreviation or Acronym

    CEPHEUS

    Country
    Name
    Belgium
    France
    Greece
    Ireland
    Finland
    Turkey
    Luxembourg
    Abstract

    Determine the proportion of patients on lipid-lowering drugs who reach the LDL-C goals recommended in guidelines.

    Kind of Data

    ['Clinical data','Participant-reported health data','Biological data']

    Unit of Analysis

    Individuals

    Scope

    Topics
    Topic Vocabulary URI
    Cardiology and vascular medicine health theme
    Hematology health theme
    cim-11 http://id.who.int/icd/entity/975345242
    Keywords
    Guidelines LDL cholesterol Lipid-lowering drugs Statins France

    Coverage

    Universe

    {
    "level_sex_clusion_I": [
    "Male",
    "Female"
    ],
    "level_age_clusion_I": [
    "Young Adult (19 to 24 years)",
    "Adult (25 to 44 years)",
    "Middle Aged (45 to 64 years)",
    "Aged (65 to 79 years)"
    ],
    "level_type_clusion_I": [
    "Patients population"
    ],
    "level_type_clusion_other": "",
    "clusion_I": "",
    "clusion_E": ""
    }

    Producers and sponsors

    Primary investigators
    Name
    Jean Ferrières
    Producers
    Name Role
    ASTRAZENECA (FRANCE) sponsor
    CENTRE HOSPITALIER UNIVERSITAIRE DE TOULOUSE (CHUT) sponsor
    Funding Agency/Sponsor
    Name
    ASTRAZENECA (FRANCE)

    Study authorization

    Agency
    Agency name
    CNIL
    CPP

    Sampling

    Sampling Procedure

    ['Other']

    Survey instrument

    Questionnaires

    Access on specific project only

    Methodology notes

    Observational Study

    Data collection

    Dates of Data Collection
    Start End
    2006 2006
    Time Method

    Cross-sectional study: one-time (excluding case-control studies)

    Mode of data collection
    • Converting or copying information into a structured record
    • Interview with the participant (including clinical)

    Study activities

    Study activities
    Study activities
    Type
    primary evaluation
    Description
    Health event/morbidity Health care consumption and services

    Data Access

    Access conditions

    Contact the principal investigator

    Availability Status

    Restricted access

    Contacts

    Contacts
    Name Email
    Jean Ferrières jean.ferrieres@univ-tlse3.fr

    Metadata production

    DDI Document ID

    FRESH-PEF6396-en

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