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Bas-Rhin Cancer Registry (Certified Registry)

France, 1975
Reference ID
FRESH-PEF215-en
Producer(s)
Michel Velten
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-PEF215-en

    Title

    Bas-Rhin Cancer Registry (Certified Registry)

    Country
    Name
    France
    Abstract
    • Registry objectives regarding public health: The registry was created in 1974 with two main aims: 1. To create a useful tool for epidemiological research and evaluation, modelled on tools established in various other countries; 2. To verify morbidity data of the unfavourable situation in Alsace with regards to high cancer mortality. The Bas-Rhin cancer registry is responsible for estimating cancer incidence, prevalence and survival. The registry also aims to participate in national and international studies in these areas: comparing incidence rates to locate different geographical regions and compare them in a database; to develop existing work to identify factors that explain variations in cancer incidence, prevalence and survival. The cancer registry is also a tool for assessing the effectiveness of preventive measures, especially screening campaigns throughout the département for breast cancer since 1989, cervical and colon cancer since 1994 and colon and rectal cancer since 2008. As such, the trend in incidence rate can be monitored and the proportion of false negatives can be documented. - Registry research objectives: The registry is developing research in the field of estimating cancer incidence in geographical areas with no registry, as well as estimating survival through relative survival and healing models in order to obtain the best "current" survival estimates.
    Kind of Data

    ['Clinical data','Socio-demographic data']

    Unit of Analysis

    Individuals

    Scope

    Topics
    Topic Vocabulary URI
    Oncology health theme
    cim-11 http://id.who.int/icd/entity/846453488
    Keywords
    tool epidemiological research assessment morbidity mortality incidence prevalence survival

    Coverage

    Geographic Coverage

    ['Grand Est']

    Universe

    {
    "level_sex_clusion_I": [
    "Male",
    "Female"
    ],
    "level_age_clusion_I": [
    "Infant (28 days to 2 years)",
    "Child, Preschool (2 to 5 years)",
    "Child (6 to 12 years)",
    "Young Adult (19 to 24 years)",
    "Adult (25 to 44 years)",
    "Middle Aged (45 to 64 years)",
    "Aged (65 to 79 years)",
    "Aged, 80 and over (80 years and more)"
    ],
    "level_type_clusion_I": [
    "Patients population"
    ],
    "level_type_clusion_other": "",
    "clusion_I": "",
    "clusion_E": ""
    }

    Producers and sponsors

    Primary investigators
    Name
    Michel Velten
    Producers
    Name Role
    LES HOPITAUX UNIVERSITAIRES DE STRASBOURG (HUS) sponsor
    Funding Agency/Sponsor
    Name
    SANTE PUBLIQUE FRANCE

    Study authorization

    Agency
    Agency name
    CNIL

    Sampling

    Sampling Procedure

    ['Other']

    Survey instrument

    Questionnaires

    Access on specific project only

    Methodology notes

    Observational Study

    Data collection

    Dates of Data Collection
    Start
    1975
    Time Method

    Morbidity registry

    Mode of data collection
    • Converting or copying information into a structured record

    Study activities

    Study activities
    Study activities
    Type
    primary evaluation
    Description
    Health event/morbidity Health event/mortality

    Data Access

    Access conditions

    Contact the principal investigator

    Availability Status

    Restricted access

    Contacts

    Contacts
    Name Email
    Michel Velten michel.velten@unistra.fr

    Metadata production

    DDI Document ID

    FRESH-PEF215-en

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