Home / Central Data Catalog / FRESH-PEF60163-EN
central

Multicentric Prospective Cohort Study of Patients with Chronic Alcoholic and/or Metabolic Liver Disease

France, 2011 - 2018
Reference ID
FRESH-PEF60163-en
Producer(s)
Victor;DE LEDINGHEN
Metadata
DDI/XML JSON
Created on
Dec 18, 2025
Last modified
Dec 18, 2025
Page views
3
  • Identification
  • Scope
  • Coverage
  • Producers and sponsors
  • Sampling
  • Survey instrument
  • Data collection
  • Study activities
  • Data Access
  • Contacts
  • Metadata production

    • Identification

    Survey ID number

    FRESH-PEF60163-en
    Title

    Multicentric Prospective Cohort Study of Patients with Chronic Alcoholic and/or Metabolic Liver Disease
    Abbreviation or Acronym

    CALMET
    Country
    Name Country code
    France fr
    Kind of Data

    ['Clinical data','Participant-reported health data','Biological data','Paraclinical data (non-biological) : Imaging','Paraclinical data (non-biological) : Anthropometry']
    Unit of Analysis

    Individuals

    Scope

    Topics
    Topic Vocabulary
    Endocrinologie health theme
    Hepatology health theme
    Hepatic cirrhosis cim-11
    Hepatocellular carcinoma of liver cim-11
    Biological determinants: Genetic predisposition health determinant
    Biological determinants health determinant
    Keywords
    decompensation liver failure portal hypertension cirrhosis gastrointestinal bleeding ascites renal failure encephalopathy guided liver biopsy Health episodes aggravation infection prevention care treatment CHC imaging diagnosis death

    Coverage

    Universe

    {
    "level_sex_clusion_I": [
    {
    "value": "Male",
    "concept": {
    "vocab": "MeSH",
    "vocabURI": "http:\/\/id.nlm.nih.gov\/mesh\/D008297"
    }
    },
    {
    "value": "Female",
    "concept": {
    "vocab": "MeSH",
    "vocabURI": "http:\/\/id.nlm.nih.gov\/mesh\/D005260"
    }
    }
    ],
    "level_age_clusion_I": [
    {
    "value": "Young Adult (19 to 24 years)",
    "concept": {
    "vocab": "MeSH",
    "vocabURI": "http:\/\/id.nlm.nih.gov\/mesh\/D055815"
    }
    },
    {
    "value": "Adult (25 to 44 years)",
    "concept": {
    "vocab": "MeSH",
    "vocabURI": "http:\/\/id.nlm.nih.gov\/mesh\/D000328"
    }
    },
    {
    "value": "Middle Aged (45 to 64 years)",
    "concept": {
    "vocab": "MeSH",
    "vocabURI": "http:\/\/id.nlm.nih.gov\/mesh\/D008875"
    }
    },
    {
    "value": "Aged (65 to 79 years)",
    "concept": {
    "vocab": "MeSH",
    "vocabURI": "http:\/\/id.nlm.nih.gov\/mesh\/D000368"
    }
    },
    {
    "value": "Aged, 80 and over (80 years and more)",
    "concept": {
    "vocab": "MeSH",
    "vocabURI": "http:\/\/id.nlm.nih.gov\/mesh\/D000369"
    }
    }
    ],
    "level_type_clusion_I": "Patients population",
    "level_type_clusion_other": "",
    "clusion_I": "",
    "clusion_E": ""
    }

    Producers and sponsors

    Primary investigators
    Name
    Victor;DE LEDINGHEN
    Producers
    Name
    CENTRE HOSPITALIER UNIVERSITAIRE DE BORDEAUX
    Funding Agency/Sponsor
    Name
    AGENCE NATIONALE DE LA RECHERCHE (ANR)
    INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM)

    Sampling

    Sample frame

    Unit Type

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

    ['{"concept":{"vocabURI":"Other","vocab":"CESSDA"},"value":"Other"}']

    Survey instrument

    Questionnaires

    Access on specific project only
    Methodology notes

    Observational Study

    Data collection

    Dates of Data Collection
    Start End
    2011-01-01 2018-01-01
    Mode of data collection
    • {"concept":{"vocabURI":"SelfAdministeredQuestionnaire","vocab":"CESSDA"},"value":"Self-administered questionnaire"}
    • {"concept":{"vocabURI":"Interview","vocab":"CESSDA"},"value":"Interview with the participant (including clinical)"}

    Study activities

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

    Data Access

    Access conditions

    Access for each nested study using clinical data and/or samples collected from the cohort is subject to specific projects that have an indicated link to the cohort. All independent aspects regarding the associated project (clinical data, questionnaires, additional tests, bioassays etc.) will require specific funding. Research projects must first be discussed and approved by the Scientific Council, either at annual meetings, or after distribution via email (if necessary). In any case, clinical data from the common database or stored biological samples can not be used in a study by a member of the Scientific Council or by an investigator (or any other persons) without the consent of the group according to the regulations stated above. In the case of a disagreement regarding the use of data or samples, voting will be carried out in order ​​to choose between the different proposals (rules to be defined). Implementation of nested studies will be subject to prior authorisation and review from the appropriate regulatory bodies.
    Availability Status

    {"value":"Restricted access","extLink":[{"title":"COAR","uri":"http://purl.org/coar/access_right/c_16ec"}]}
    Restrictions

    Data may be used by academic teams. Data may not be used by industrial teams.

    Contacts

    Contacts
    Name Email
    Victor;DE LEDINGHEN victor.deledinghen@chu-bordeaux.fr

    Metadata production

    DDI Document ID

    FRESH-PEF60163-en
    Back to Catalog