Recall of Information on Intravenous Thrombolysis in Acute Ischaemic Stroke Patients Given During Informed Consent: a Prospective Observational Study.
Trial Snapshot
- Phase
- Not Applicable
- Enrollment
- 260
- Locations
- 5
- Primary Endpoint
- Recall of the designated facts given during informed consent procedure on intravenous thrombolysis after acute ischaemic stroke
Study Overview
Brief 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).
Study Design
- Study Type
- Observational
- Observational Model
- Other
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Not provided
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
Recall of the designated facts given during informed consent procedure on intravenous thrombolysis after acute ischaemic stroke
Time Frame: Within 24 hours
Secondary Outcomes
No secondary outcomes reported
Investigators
Karl Georg Haeusler
Consultant Neurologist
Wuerzburg University Hospital