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NCT03571763Recruiting

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

The Impact of Anti-thrombosis on Cerebral Microbleeds and Intracranial Hemorrhage in Ischemic Stroke Patients: Prospective, Multi-center, Cohort Study

Source: ClinicalTrials.gov · Last updated 27 Apr 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
1875 (estimated)
First submitted
5 Jun 2018
Start date
1 Aug 2018
Primary completion date
30 Dec 2026
Lead sponsor
General Hospital of Shenyang Military Region
Diseases
Stroke
NCT number
NCT03571763

What you commit to

  • Study type: Observational
  • Planned participants: 1875
  • From 1 Aug 2018 to the primary completion date, 30 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Contraindication for antiplatelet or anticoagulation therapy;

Other illness

  • Hemorrhagic transformation after acute Ischemic stroke;
  • Severe head trauma or intracranial hemorrhage occurred in the past six months;

Other

  • MRI contraindication;
  • obvious coagulopathy;
  • Other intracranial lesions associated with (such as tumor, cerebral vascular malformation);
  • other unqualified patients judged by the investigator

Who the study is looking for

  • Patient age ≥18 years;
  • Acute ischemic stroke patient confirmed by imaging;
  • Time of onset: within 3 months;
  • Baseline SWI sequence is completed before starting the secondary prevention of ischemic stroke;
  • Baseline SWI sequence must have at least one CMB ;
  • NIHSS≤10

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
General Hospital of ShenYang Military Region
Coordinator of this site? Confirm its status
ShenyangChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.