Prospective Cohort With Incident Stroke
Status: Recruiting
Location: See all (2) locations...
Study Type: Observational
SUMMARY
The primary aim of the study is to derive and validate risk scores for vascular endpoints (recurrent stroke, myocardial infarction, and other complications of stroke) and for death following an incident stroke. For this purpose patients with an incident stroke will be followed for 36 months with additional assessments at 3, 12, 24 and 36 months.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• Age ≥18 years
• Language: German
• First ever acute ischemic stroke that occurred with stroke onset in the last 7 days
• Written informed consent by patient prior to study participation
• Willingness to participate in follow-up
Locations
Other Locations
Germany
Center for Stroke Research Berlin, Charité Universitätsmedizin Berlin
ACTIVE_NOT_RECRUITING
Berlin
Interdisciplinary Stroke Center Munich, Klinikum der Universität München
RECRUITING
Munich
Contact Information
Primary
Martin Dichgans, Prof.
martin.dichgans@med.uni-muenchen.de
+49 (0)89 4400
Time Frame
Start Date: 2011-02
Estimated Completion Date: 2027-12
Participants
Target number of participants: 850
Treatments
First ever acute ischemic stroke
Patients over 18 years and without prior stroke according to WHO criteria, displaying an ischemic stroke, onset within the last 7 days, language German
Authors
Related Therapeutic Areas
Sponsors
Leads: Ludwig-Maximilians - University of Munich
Collaborators: Charite University, Berlin, Germany