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A European prospective observational study to evaluate fracture outcomes, back pain, health-related quality of life, and compliance in patients with osteoporosis during and after treatment with Forsteo®

Croatia, Denmark, France...and 5 more, 2006 - 2012
Reference ID
FRESH-PEF79-en
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
  • Metadata production
  • Identification

    Survey ID number

    FRESH-PEF79-en

    Title

    A European prospective observational study to evaluate fracture outcomes, back pain, health-related quality of life, and compliance in patients with osteoporosis during and after treatment with Forsteo®

    Abbreviation or Acronym

    EXFOS

    Country
    Name
    Croatia
    Denmark
    France
    Greece
    Italy
    Norway
    Slovenia
    Sweden
    Abstract

    Primary objective: determine the incidence of clinical vertebral fractures and non-vertebral fragility fractures in patients treated with teriparatide for about 18 months and a post-treatment follow-up period of at least 18 months. Secondary objectives: observance, treatment switching and cessation, clinical evolution, occurrence of back pain, direct costs linked to fractures.

    Kind of Data

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

    Unit of Analysis

    Individuals

    Scope

    Topics
    Topic Vocabulary URI
    Rheumatology health theme
    cim-11 XS65
    Healthcare system determinants: Use of care health determinant
    Healthcare system determinants health determinant
    Keywords
    Osteoporotic patients teriparatide duration of treatment conditions of use

    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)",
    "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

    Producers
    Name Role
    LILLY FRANCE sponsor
    Funding Agency/Sponsor
    Name
    LILLY FRANCE

    Study authorization

    Agency
    Agency name
    CNIL

    Sampling

    Sample frame

    Unit Type

    ['Through independent healthcare practitioners']

    Sampling Procedure

    ['Other']

    Survey instrument

    Questionnaires

    Access on specific project only

    Methodology notes

    Observational Study

    Data collection

    Dates of Data Collection
    Start End
    2006 2012
    Time Method

    Longitudinal or cohort study

    Mode of data collection
    • Interview with the participant (including clinical)

    Study activities

    Study activities
    Study activities
    Type
    primary evaluation
    Description
    Health event/morbidity Health care consumption and services Quality of life/health perception

    Data Access

    Availability Status

    Restricted access

    Metadata production

    DDI Document ID

    FRESH-PEF79-en

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