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Cancer Registry of the Manche (qualified registry)

France, 1994 - 2008
Reference ID
FRESH-PEF214-en
Producer(s)
Simona Bara
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-PEF214-en

    Title

    Cancer Registry of the Manche (qualified registry)

    Country
    Name
    France
    Abstract

    The Registry of Cancers for la Manche was created in 1994. It stems from a local medical need, in order to supplement the incidence rates measured in the neighboring département of Calvados and to answer the public health questions raised by the industrial activity in the département (the nuclear industry predominantly and the use of asbestos in civil and military ship building). The registry performs a permanent and complete collection of all of the new diagnoses of cancer in the general population residing in the département of la Manche. It has a dual objective of describing and monitoring the risk of cancer and of conducting research using the analysis of the data collected or one-off surveys. Objectives of the Registry in terms of public health: - Participate in the epidemiological monitoring of cancers on a local and national level within the framework of the Francim network, through publishing incidence indicators by cancer location, sex, age and year of diagnosis. - Contribute to assessing primary and secondary prevention initiatives (organized cancer screenings), caring for patients and the care needs for the general population.

    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

    Coverage

    Geographic Coverage

    ['Normandie']

    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
    Simona Bara
    Producers
    Name Role
    CENTRE HOSPITALIER PUBLIC DU COTENTIN sponsor
    Funding Agency/Sponsor
    Name
    ASS REGISTRE CANCERS DEP MANCHE (ARKM)
    INSTITUT NATIONAL DU CANCER (INCA)
    SANTE PUBLIQUE FRANCE

    Study authorization

    Agency
    Agency name
    CNIL

    Sampling

    Sample frame

    Unit Type

    ['Through organizations (health services or institutions, schools, businesses, etc.)']

    Sampling Procedure

    ['Other']

    Survey instrument

    Questionnaires

    Access on specific project only

    Methodology notes

    Observational Study

    Data collection

    Dates of Data Collection
    Start End
    1994 2008
    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

    The data recorded in the Registry database can be used for specific studies. The methods for collaboration have to be defined.

    Availability Status

    Restricted access

    Contacts

    Contacts
    Name Email
    Simona Bara s.bara@ch-cherbourg.fr

    Metadata production

    DDI Document ID

    FRESH-PEF214-en

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