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Patient Acceptable Symptomatic State

France, 2009 - 2010
Reference ID
FRESH-PEF93-en
Producer(s)
Franck;VIGNAL
Metadata
DDI/XML JSON
Study website Interactive tools
Created on
Feb 18, 2026
Last modified
Feb 18, 2026
Page views
91
  • Study Description
  • Get Microdata
  • Identification
  • Scope
  • Coverage
  • Producers and sponsors
  • Study authorization
  • Sampling
  • Survey instrument
  • Data collection
  • Study activities
  • Data Access
  • Contacts
  • Identification

    Survey ID number

    FRESH-PEF93-en

    Title

    Patient Acceptable Symptomatic State

    Abbreviation or Acronym

    PASS-ARTHROSE

    Country
    Name Country code
    France fr
    Kind of Data

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

    Unit of Analysis

    Individuals

    Scope

    Topics
    Topic Vocabulary
    Rheumatology health theme
    Osteoarthritis cim-11
    Behavioral determinants health determinant
    Keywords
    evaluation of the pain and response to antalgic treatment PASS Minimal Clinically Important Improvement (MCII)

    Coverage

    Universe

    {"level_sex_clusion_I":[{"value":"Male","concept":{"vocab":"MeSH","vocabURI":"D008297"}},{"value":"Female","concept":{"vocab":"MeSH","vocabURI":"D005260"}}],"level_age_clusion_I":[{"value":"Middle Aged (45 to 64 years)","concept":{"vocab":"MeSH","vocabURI":"D008875"}},{"value":"Aged (65 to 79 years)","concept":{"vocab":"MeSH","vocabURI":"D000368"}},{"value":"Aged, 80 and over (80 years and more)","concept":{"vocab":"MeSH","vocabURI":"D000369"}}],"level_type_clusion_I":"Patients population","level_type_clusion_other":"","clusion_I":"Patients must: • be ambulatory, • be aged 50 years or older, • consult for a defined gonarthrosis and/or coxarthrosis according to the clinical or radiological criteria of the American College of Rheumatology, • be symptomatic with pain greater or equal to 3 on a numerical pain scale from 0 to 10, at rest or during movement, in the 24 hours preceding entry in the study, • requiring the taking of an antalgic treatment for a duration of at least one week, • be able and accept to complete a self-evaluation questionnaire, • accepting to participate in the survey.","clusion_E":""}

    Producers and sponsors

    Primary investigators
    Name
    Franck;VIGNAL
    Producers
    Name Role
    SANOFI (FRANCE) sponsor
    Funding Agency/Sponsor
    Name
    AGENCE NATIONALE DE RECHERCHES SUR LE SIDA ET LES HEPATITES VIRALES (ANRS MIE)

    Study authorization

    Agency
    Agency name
    CNIL
    CPP

    Sampling

    Sample frame

    Unit Type

    ['Medical-administrative database (patients, health insurance/mutual insurance)','Disease and death registry','Through independent healthcare practitioners']

    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
    2009-01-01 2010-01-01
    Time Method

    One-time cross-sectional study

    Mode of data collection
    • {"concept":{"vocabURI":"SelfAdministeredQuestionnaire","vocab":"CESSDA"},"value":"Self-administered questionnaire"}

    Study activities

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

    Data Access

    Availability Status

    {"value":"To be defined","extLink":[]}

    Contacts

    Contacts
    Name Email
    Franck;VIGNAL franck.vignal@sanofi.com
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