I63
Conditions
Interventions
Group 1: Acute stroke patients with known atrial fibrillation receive standard care. Data on acute management and past medical history is extracted from routine clinical notes. Data on 90-day outcomes
Sponsors
Universitätsklinikum Hamburg-Eppendorf
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Clinical diagnosis of acute ischemic stroke Stroke symptom onset within 24 hours prior to presentation Known diagnosis of atrial fibrillation Treatment on a certified German Stroke Unit or Neuro-Intensive Care Unit
Exclusion criteria
Exclusion criteria: First diagnosis of atrial fibrillation in-hospital Participation in a randomized acute stroke trial with concealed treatment allocation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Functional outcome (modified Rankin Scale) after 3 months | — |
Secondary
| Measure | Time frame |
|---|---|
| Symptomatic intracranial hemorrhage (mSITS-MOST) within 36 hours | — |
Countries
Germany
Contacts
Public ContactEckhard Schlemm
Universitätsklinikum Hamburg-Eppendorf
Outcome results
None listed