跳至主要内容
临床试验/NCT03246256
NCT03246256Unknown不适用

Recall of Information on Intravenous Thrombolysis in Acute Ischaemic Stroke Patients Given During Informed Consent: a Prospective Observational Study.

Charite University, Berlin, Germany5 个研究点 分布在 1 个国家目标入组 260 人开始时间: 2016年12月21日最近更新:
适应症

试验速览

阶段
不适用
入组人数
260
试验地点
5
主要终点
Recall of the designated facts given during informed consent procedure on intravenous thrombolysis after acute ischaemic stroke

研究概览

简要总结

The aim of the study is to investigate the ability to recall information given during informed consent on intravenous thrombolysis in patients with acute ischaemic stroke.

详细描述

The purpose of this prospective multi-center study is to investigate whether patients with acute ischaemic stroke are able to recall information given before providing informed consent to intravenous thrombolysis after the end of treatment. Patients with acute ischaemic stroke will be compared to a group of relatives who witnessed the informed consent procedure of a relative with acute ischaemic stroke, stroke patients who were not treated with intravenous thrombolysis and patients without an ischaemic stroke but similiar risk factors (admitted to the Departement of Cardiology and Pneumology, Charité, Campus Benjamin Franklin, Berlin, Germany).

研究设计

研究类型
Observational
观察模型
Other
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

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Recall of the designated facts given during informed consent procedure on intravenous thrombolysis after acute ischaemic stroke

时间窗: Within 24 hours

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Karl Georg Haeusler

Consultant Neurologist

Wuerzburg University Hospital

研究点 (5)

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