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Predictive Value of Infarction Volume on Hemorrhagic Transformation in Ischemic Stroke/TIA With Non-valve Atrial Fibrillation(NVAF) Patients Using Rivaroxaban

Zhejiang University logo

Zhejiang University

Status

Enrolling

Conditions

Intracranial Hemorrhages
Cerebrovascular Stroke
Anticoagulant
Matrix Metalloproteinases

Treatments

Drug: Rivaroxaban

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT03772457
InV HT RAF 1010

Details and patient eligibility

About

This study was aimed at patients with newly diagnosed stroke / TIA associated with nonvalvular atrial fibrillation. We will observe the effect of early using rivaroxaban anticoagulation on hemorrhagic transformation, and explore the predictive value of multi-mode MRI infarct volume / MMP-9 on hemorrhagic transformation after anticoagulation therapy.

Enrollment

400 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Male or female, age≥18;
  2. Were newly diagnosed asischemic stroke/TIA concomitant NVAF;
  3. Prescribedand accept Rivaroxaban;
  4. Sign thewritten informed consent.

Exclusion criteria

  1. Renal impairment (CrCl<15 ml/min) or severe hepatic impairment.
  2. Significant hemorrhagic transformation (parenchymal hematoma type I or type II by the ECASS definition).
  3. Stroke or TIA caused by large artery atherosclerosis
  4. Planned major surgery or invasive intervention
  5. Active internal bleeding
  6. Malignancy or other serious medical conditions with a life expectancy <6 months
  7. Allergery to Rivaroxaban
  8. Pregnancy or breast-feeding

Trial contacts and locations

1

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Central trial contact

Min Lou, PhD

Data sourced from clinicaltrials.gov

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