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ARAMIS Registry: Addressing Anticoagulant Management Issues in Stroke

Clinical Trial Title: 
ARAMIS Registry: Addressing anticoagulant management issues in stroke.
Clinical Trial Protocol ID: 
Clinical Trial Investigator Name: 
James Conners, MD
Clinical Trial Protocol Description: 

The ARAMIS Registry is a multicenter, prospective, observational study of acute ischemic stroke (AIS) and intracerebral hemorrhage (ICH) patients on home anticoagulation therapy.

Clinical Trial Eligibility Criteria: 

In order to participate you must meet the following criteria:

  • Be 18 years of age or older.
  • Are diagnosed with AIS and on dabigatran, rivaroxaban, apixaban or edoxaban prior to admission.
  • Are diagnosed with ICH and on warfarin or one of the new oral anticoagulats prior to admission.

You will be excluded from the study if any of the following criteria apply to you:

  • Were transferred from another hospital or discharged to another acute care facility.

This is a partial list of inclusion and exclusion criteria.

Clinical Trial Area: 
Stroke and Cerebrovascular Disease
Contact Phone: 
(312) 563-2208
Contact Name: 
Tiffany Singson