Actively Recruiting

Age: 18Years +
All Genders
NCT03571763

The Impact of Anti-thrombosis on Cerebral Microbleeds and Intracranial Hemorrhage in Ischemic Stroke Patients

Led by General Hospital of Shenyang Military Region · Updated on 2026-04-27

1875

Participants Needed

1

Research Sites

439 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this prospective cohort study is to investigate whether antithrombotic therapy in the secondary prevention of ischemic stroke increases the risk of the emerging CMBs and whether the change is associated with an increased risk of intracranial hemorrhage, providing an imaging evidence for individualized antithrombotic therapy in such patients.

CONDITIONS

Official Title

The Impact of Anti-thrombosis on Cerebral Microbleeds and Intracranial Hemorrhage in Ischemic Stroke Patients

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient age 18 years or older
  • Acute ischemic stroke confirmed by imaging
  • Stroke onset within 3 months
  • Baseline susceptibility weighted imaging (SWI) done before starting secondary prevention
  • At least one cerebral microbleed visible on baseline SWI
  • NIH Stroke Scale (NIHSS) score of 10 or less
Not Eligible

You will not qualify if you...

  • Contraindication to MRI
  • Hemorrhagic transformation after acute ischemic stroke
  • Contraindication for antiplatelet or anticoagulation therapy
  • Severe head trauma or intracranial hemorrhage within the past 6 months
  • Obvious coagulopathy
  • Other intracranial lesions such as tumor or cerebral vascular malformation
  • Other conditions deemed unqualified by the investigator

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

General Hospital of ShenYang Military Region

Shenyang, China

Actively Recruiting

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Research Team

C

chen huisheng, doctor

CONTACT

W

wang xinhong, doctor

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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