Clinical Trials Directory

Trials / Unknown

UnknownNCT03246256

Information Recall on Informed Consent to Intravenous Thrombolysis in Patients With Acute Ischaemic Stroke.

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

Status
Unknown
Phase
Study type
Observational
Enrollment
260 (estimated)
Sponsor
Charite University, Berlin, Germany · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed 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).

Conditions

Interventions

TypeNameDescription
OTHERGroup 1

Timeline

Start date
2016-12-21
Primary completion
2020-06-01
Completion
2021-06-01
First posted
2017-08-11
Last updated
2020-11-13

Locations

5 sites across 1 country: Germany

Source: ClinicalTrials.gov record NCT03246256. Inclusion in this directory is not an endorsement.