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临床试验/NCT07723950
NCT07723950尚未招募不适用

Development and Validation of Algorithms for Identifying Intracerebral Hemorrhage and Seizures in Patients With Alzheimer's Disease: A Retrospective Database Study Using United States Healthcare Administrative Claims Data

Eisai Inc.0 个研究点目标入组 600 人开始时间: 2026年7月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
Eisai Inc.
入组人数
600
主要终点
Positive Predictive Value (PPV) of algorithms to identify intracerebral hemorrhage >1 cm in diameter

研究概览

简要总结

The primary objective of this study is to develop and validate claims-based algorithms to identify intracerebral hemorrhage >1 cm in diameter, ensuring differentiation from amyloid-related imaging abnormality-microhemorrhage and hemosiderin deposit (ARIA-H; microhemorrhage, superficial siderosis) in participants with Alzheimer's disease (AD) using claims data in the United States (US) with linkage to electronic health records (EHRs), and to estimate the positive predictive values (PPVs) of the algorithms. The secondary objective of the study is to validate claims-based algorithms to identify new-onset seizures in participants with AD using US claims data with linkage to EHRs and to estimate the PPVs of the algorithms.

详细描述

As this is a Retrospective Database Study, the Study Start Date for this study references the date at which the first set of data will become available.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Before or on the outcome event date, have at least 1 ICD-10-CM diagnosis code for AD in medical claims in an inpatient setting; or have at least 2 ICD-10-CM diagnosis codes in medical claims in an outpatient setting, at least 7 days and less than 365 days apart
  • Have at least 365 days of continuous coverage with medical and pharmacy benefits before the outcome event date
  • Have EHR data available for (1) the outcome event date or (2) during the period of up to 30 days before and up to 90 days after the outcome event date
  • Have unstructured EHR information (ie, clinical notes) available for any encounter (1) on the outcome event date or (2) during the period of 30 days before to up to 45 days after the outcome event date

排除标准

  • New-onset seizure outcome only: Have any ICD-10-CM diagnosis code for seizure or epilepsy before the outcome event date

研究组 & 干预措施

Alzheimer's Disease Participants in US Claims-EHR Data

干预措施: No intervention (Other)

结局指标

主要结局

Positive Predictive Value (PPV) of algorithms to identify intracerebral hemorrhage >1 cm in diameter

时间窗: Up to 9.5 years

次要结局

  • PPV of algorithms to identify new-onset seizure(Up to 9.5 years)

研究者

发起方
Eisai Inc.
申办方类型
Industry
责任方
Sponsor

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