{"doc_desc":{"title":"Etude longitudinale europ\u00e9enne sur des patients ost\u00e9oporotiques initiant un traitement par t\u00e9riparatide (Forsteo\u00ae) : fractures, rachialgies, qualit\u00e9 de vie et observance","idno":"FRESH-PEF79-fr","producers":[{"name":"","affiliation":""}]},"study_desc":{"title_statement":{"idno":"FRESH-PEF79-fr","IDno":{"metadata_no":[{"agency":"PEF","code":"79"},{"agency":"FReSH","code":"FRESH-PEF79"}]},"title":"Etude longitudinale europ\u00e9enne sur des patients ost\u00e9oporotiques initiant un traitement par t\u00e9riparatide (Forsteo\u00ae) : fractures, rachialgies, qualit\u00e9 de vie et observance","alternate_title":"ExFOS : Extended Forsteo\u00ae Observational Study"},"study_authorization":{"agency":[{"name":"CNIL"}]},"authoring_entity":[],"oth_id":[{"name":""}],"production_statement":{"prod_place":"Portail Epid\u00e9miologie France (PEF)","producers":[{"name":"LILLY FRANCE","extlink":[{"title":"SIREN","uri":"609849153","role":"sponsor id"}],"role":"sponsor"}],"funding_agencies":[{"name":"AGENCE NATIONALE DE RECHERCHES SUR LE SIDA ET LES HEPATITES VIRALES (ANRS MIE)","extlink":[{"title":"SIREN","uri":"609849153"}]}]},"distribution_statement":{"contact":[{"name":"","type":"contact"}]},"study_info":{"keywords":[{"keyword":"Patientes ost\u00e9oporotiques"},{"keyword":"t\u00e9riparatide"},{"keyword":"dur\u00e9e du traitement"},{"keyword":"conditions d'utilisation"}],"topics":[{"topic":"Rhumatologie","vocab":"health theme","extLink":[{"title":"ESV","uri":"http:\/\/data.europa.eu\/8mn\/euroscivoc\/bfb0bafd-7894-45ba-84fc-ddab5fd6c537"},{"title":"MeSH","uri":"http:\/\/id.nlm.nih.gov\/mesh\/D012219"}]},{"topic":"D\u00e9terminants li\u00e9s au syst\u00e8me de sant\u00e9 : Consommation des soins","vocab":"health determinant"},{"topic":"D\u00e9terminants li\u00e9s au syst\u00e8me de sant\u00e9","vocab":"health determinant"}],"purpose":"Objectif principal : d\u00e9terminer l\u2019incidence des fractures cliniques vert\u00e9brales et des fractures non vert\u00e9brales de fragilit\u00e9 osseuse chez des patients trait\u00e9s par t\u00e9riparatide pendant une dur\u00e9e de traitement d\u2019environ 18 mois et une p\u00e9riode de suivi post-traitement d\u2019une dur\u00e9e d\u2019au moins 18 mois. 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