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NCT number NCT03246256
Study type Observational
Source Charite University, Berlin, Germany
Contact Karl Georg Häusler, MD
Phone +49 30 450 560 676
Email georg.haeusler@charite.de
Status Recruiting
Phase N/A
Start date December 21, 2016
Completion date December 2018

Clinical Trial Summary

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.


Clinical Trial Description

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).


Study Design


Related Conditions & MeSH terms


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