Prospective Cohort With Incident Stroke

Recruiting Observational Study
Ischemic Stroke
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
850 (estimated)
Sponsor
Ludwig-Maximilians - University of Munich · Other
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About This Trial

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.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * 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 Exclusion Criteria: * Prior stroke (definition …
Contacts

Martin Dichgans, Prof.

+49 (0)89 4400

martin.dichgans@med.uni-muenchen.de

CONTACT