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Clinical Trial Summary

This multicenter international prospective cohort study will include patients with AIS with a known or newly diagnosed anticoagulant-naïve AF. All centers will use the same transcranial Doppler machine for one-hour monitoring with bilateral 2-MHz probes within 24 hours of symptom onset. Recordings will be analyzed for MES by a blinded central reader. The primary aim is to determine the proportion of patients with MES and the association of MES with functional outcomes assessed by a modified Rankin scale (mRS) score at 90 days.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06018090
Study type Observational [Patient Registry]
Source Centro Hospitalar De São João, E.P.E.
Contact
Status Completed
Phase
Start date June 6, 2019
Completion date October 6, 2022

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