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临床试验/NCT05669456
NCT05669456尚未招募不适用

Zeit Alert for Stroke at Home (ZASH) Protocol

Zeit Medical, Inc.0 个研究点目标入组 300 人开始时间: 2023年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
300
主要终点
Feasibility of Halo Alert System to collect EEG data for algorithm development

研究概览

简要总结

This is a single-arm, observational, feasibility study to evaluate if the Halo Alert System can be used in the future to detect stroke events in individuals at risk for stroke wearing the Halo Alert System overnight.

详细描述

This is a single-arm, observational, feasibility study to evaluate if the Halo Alert System can be used in the future to detect stroke events in individuals at risk for stroke wearing the Halo Alert System overnight. The Halo Alert System consists of an EEG sensor headband and is paired with a data transfer device. Approximately 300 subjects with elevated stroke risk will be enrolled and followed for a duration of 90 days. The EEG tracing for each study subject will be labeled after study conclusion with the help of clinically available information on the occurrence of a recurrent stroke. The labeled data will then be used to further develop the existing (operating room based) stroke detection algorithm and adjust the algorithm for outpatient use.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • New ischemic stroke confirmed by neuroimaging (CT or MRI scans) as the reason for current hospital admission or stroke clinics visit. Time from ictus to enrollment should be ≤ 2 weeks;
  • RRE-90 > 2;
  • Age ≥ 18 years old;
  • Patient is discharged to home;
  • Provision of signed and dated informed consent form.

排除标准

  • Subject is a member of a vulnerable population, such as prisoners, individuals without legal papers, or otherwise exploitable population;
  • Treatment with another investigational drug or intervention within the last two (2) weeks prior to start of this study, if said drug/intervention is expected to interfere with the normal function of the Halo Alert System;
  • Does not have WIFI internet access in their home;
  • Does not have access to a smartphone;
  • Open traumatic injury on the head;
  • Allergy to any of the components of the headband, such as the fabric of the band (88% Rayon, 9% Nylon, 3% Spandex), the electrode surfaces (conductive silver ink.)

结局指标

主要结局

Feasibility of Halo Alert System to collect EEG data for algorithm development

时间窗: 12 months enrollment period

Subject's data collection with the Halo Alert System to assess the feasibility of EEG based stroke detection at home for algorithm development.

次要结局

未报告次要终点

研究者

发起方
Zeit Medical, Inc.
申办方类型
Industry
责任方
Sponsor

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Zeit Alert for Stroke at Home (ZASH) Protocol | 临床试验