{"id":33605,"date":"2022-04-12T11:21:17","date_gmt":"2022-04-12T09:21:17","guid":{"rendered":"https:\/\/www.treatswitzerland.org\/home\/"},"modified":"2025-06-12T09:49:14","modified_gmt":"2025-06-12T07:49:14","slug":"home","status":"publish","type":"page","link":"https:\/\/www.treatswitzerland.org\/en\/","title":{"rendered":"Home"},"content":{"rendered":"\n
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For patients<\/h2>\n\n\n\n

Information on objectives, inclusion criteria, and procedures of the registry study.<\/p>\n\n\n\n

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I am patient<\/a><\/div>\n<\/div>\n<\/div>\n\n\n\n
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For doctors<\/h2>\n\n\n\n

Information on the registry study, study management, and study centers.<\/p>\n\n\n\n

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I am doctor<\/a><\/div>\n<\/div>\n<\/div>\n<\/div>\n\n

TREATswitzerland<\/h2>\n\n
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TREATswitzerland is the patient registry for atopic dermatitis (neurodermatitis) in Switzerland. To date, there is a lack of accurate data on the medical care of patients with atopic dermatitis, the course of the disease and response to treatment, and the impact on quality of life. In an observational study of patients with moderate and severe atopic dermatitis, data will be collected and scientifically evaluated (observational cohort study).<\/p>\n\n\n\n

This objective of the registry study should be reflected in the illustrations.\nWe also want to give the patients a face – to show the burden that atopic dermatitis brings with it, as well as the positive effect of effective therapy. <\/p>\n\n\n\n

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To the register<\/a><\/div>\n<\/div>\n<\/div>\n
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News<\/h2>\n
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\n 12. February 2026 | News\n <\/div>\n \n

Bruno Bloch Poster Prize 2025, for the first results of the TREATswitzerland Register<\/h3>\n <\/a>\n <\/div>\n
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\n 17. December 2025 | News\n <\/div>\n \n

Publication Poster Prize 2025<\/h3>\n <\/a>\n <\/div>\n
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\n 07. August 2025 | News\n <\/div>\n \n

New study center opened in Geneva<\/h3>\n <\/a>\n <\/div>\n
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\n 07. April 2025 | News\n <\/div>\n \n

New study center in Zurich<\/h3>\n <\/a>\n <\/div>\n <\/div>","protected":false},"excerpt":{"rendered":"

TREATswitzerland TREATswitzerland is the patient registry for atopic dermatitis (neurodermatitis) in Switzerland. To date, there is a lack of accurate data on the medical care of patients with atopic dermatitis, the course of the disease and response to treatment, and the impact on quality of life. 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