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临床试验/NCT06587763
NCT06587763撤回不适用

Late Biomarkers in Adult Survivors After Out-of-hospital Cardiac Arrest

Region Skane3 个研究点 分布在 1 个国家目标入组 400 人开始时间: 2025年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
发起方
Region Skane
入组人数
400
试验地点
3
主要终点
Functional outcome

研究概览

简要总结

Blood samples are collected at six months follow-up from adult survivors after out-of-hospital cardiac arrest. Patients will be informed about the study and if they consent to participation, venous blood will be drawn by authorised medical personnel. Plasma, serum and PAX-RNA will be collected (ca 15 ml in total), processed and frozen for analysis after trial completion.

详细描述

Blood samples are collected at six months follow-up from adult survivors after out-of-hospital cardiac arrest. Patients will be informed about the study and if they consent to participation, venous blood will be drawn by authorised medical personnel. Plasma, serum and PAX-RNA will be collected (ca 15 ml in total), processed and frozen for analysis after trial completion.

Samples will be analysed in batch for biomarkers of brain injury, inflammation etc.

Primary outcome is functional outcome (modified Rankin Scale 4-6) at six months after cardiac arrest.

Secondary outcomes are neurocognitive function according to the Montreal Cognitive Assessment (MoCA), Symbol Digits Modalities Test (SDMT).

研究设计

研究类型
Observational
观察模型
Cohort
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

  • Survivors of out-of-cardiac arrest who participate in the extended follow-up study of the STEPCARE trial at selected sites only

排除标准

  • Patients not participating in the extended follow-up at participating sites

结局指标

主要结局

Functional outcome

时间窗: 6 months

Modified Rankin Scale 4-6

次要结局

  • Neurocognitive outcomes(6 months)

研究者

发起方
Region Skane
申办方类型
Other
责任方
Sponsor

研究点 (3)

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