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The registry collects clinical data in a secure manner that allows interoperability with other registries.
The New Hampshire Colonoscopy Registry collects detailed data from colonoscopies statewide, by using a uniform preparation quality scale after the endoscopist has cleaned the mucosa.
The location registry collects all variables and their locations that occur in the pattern that have to be checked for consistency.
The Finnish registry collects data for all ICU admissions.
The registry collects over 300 data elements for approximately 45,000 births per year.
The CORRONA registry collects longitudinal, "real-world" data from patients and their treating physicians.
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Design: a prospective voluntary registry collecting demographic and risk factor data, details of aneurysm morphology, procedure performed, immediate and 30-day outcomes.
This registry collected data prospectively from collaborating trauma centers.
A web-based registry collected retrospective data on patients with TNFRSF1A sequence variants and inflammatory symptoms.
The SEER tumor registry collected information from about 10% of all breast cancer cases in the USA.
The cancer registry collected reports from each regional hospital or local clinical oncology departments of the county hospitals.
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