Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Stroke Ischemic
Type
Interventional
Phase
Phase 3
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: None (Open Label)Masking Description: Blinded endpoint assessment by independent CECPrimary Purpose: Prevention

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

Three DOACs with marketing authorisation in Switzerland and the EU for the prevention of stroke and systemic embolism in patients with atrial fibrillation can be used. Eligible patients will be randomly assigned to either the control (antiplatelet) or the experimental (DOAC) arm with a ratio of 1:1....

Three DOACs with marketing authorisation in Switzerland and the EU for the prevention of stroke and systemic embolism in patients with atrial fibrillation can be used. Eligible patients will be randomly assigned to either the control (antiplatelet) or the experimental (DOAC) arm with a ratio of 1:1. Each study participant will be observed during a follow up period within one year after index stroke.

Tracking Information

NCT #
NCT03961334
Collaborators
Swiss National Science Foundation
Investigators
Principal Investigator: Mira Katan, PD Dr. med. University of Zurich