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Microembolic Detection in Acute Ischemic Stroke Patients With Atrial Fibrillation and Outcome

C

Centro Hospitalar De São João, E.P.E.

Status

Completed

Conditions

Atrial Fibrillation
Embolism
Infarction, Brain

Treatments

Other: The presence and rate of MES measured by TCD monitoring

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Enrollment

61 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • acute ischemic stroke admitted to the Stroke Unit, history of AF/flutter or a new diagnosis of AF at the stroke, and with a possibility to be monitored within 24 hours after symptom onset.

Exclusion criteria

  • use of anticoagulants at stroke onset; prosthetic valves; inadequate temporal bone window; uncooperative patients.

Trial design

61 participants in 1 patient group

Acute Ischemic Stroke Patients with Atrial Fibrillation
Treatment:
Other: The presence and rate of MES measured by TCD monitoring

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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