a database that records and tracks core outcomes for a specific disease or condition. Core outcomes are those that are considered the most important to measure in clinical trials and research studies, as they provide the most relevant information for patients, healthcare providers, and other stakeholders. The purpose of a core outcome registry is to promote consistency in the measurement and reporting of outcomes across different studies, as well as to facilitate comparisons and meta-analyses of results. By tracking core outcomes in a centralized database, researchers and healthcare providers can better understand the effectiveness of different treatments and interventions, and identify areas for further research and improvement.

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