Czech Neuroendocrine Registry - First Results Abstract #185

Introduction: The Czech Neuroendocrine Registry was started in October 2009 as a platform that should facilitate the data based on communication among various specialists treating NETs.
Aim(s): Well-controlled registration of patients with NETs with their risks and prognostic factors, therapeutic strategy and associated therapeutic results.
Materials and methods: Non-interventional, epidemiological, multicenter clinical registry with fully standardized clinical records, using electronic CRF, managed through on-line accessible forms. Data are collected as anonymous records with encrypted personal data of patients. All data collected concern the diagnosis of NETs. There is no recruitment of patients.
Conference: 8th Annual ENETS Conference (2011)
Category: Clinical
Presenting Author: MD Jaroslava Barkmanova

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