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NCT Number: NCT03749057

Early Rivaroxaban for Acute Ischemic Stroke or TIA Patients With Atrial Fibrillation

Anticoagulant treatment for non-valvular atrial fibrillation (AF) associated with cerebral infarction/ TIA is one of the recognized treatment of stroke prevention. The ACC/AHA and national guidelines for the management of anticoagulation recommend that most of AF patients with cerebral infarction or TIA should be administrated anticoagulant therapy within 14 days of symptom onset, while European guidelines recommend that the timing of the initiation of non-vitamin K antagonist oral anticoagulants (NOACs) for AF patients with cerebral infarction or TIA is association with stroke severity in light of the "1-3-6-12" principle. However, there are still many problems about the use of NOACs in ischemic stroke with AF. for example, it is unclear what time to begin NOACs as to difference in stroke severity, ages, comorbidity with hypertension, diabetes, heart failure, liver and kidney dysfunction and bleeding risks. Thus, the timing of the initiation of NOACs is yet to be further studied. Current urgent need is to develop a guideline-based specific regimen in which the benefit-risk factors are further balanced with a combination of NHISS, CHA2DS2-VASC and HAS-BLED score.

Rivaroxaban, a direct coagulation factor Ⅹa inhibitor, blocks the formation of the clot. ROCKET-AF study has shown that the efficacy of rivaroxaban is not inferior to that of warfarin in AF patients on stroke prevention, and rivaroxaban has a significantly decreased bleeding risk compared with warfarin. Recent study indicates that early administration with rivaroxaban for AF patients within 14 days of onset does not significantly increase hemorrhagic transformation. However, the relevant clinical data of the efficacy and safety of early initiation of rivaroxaban in AF patients with cerebral infarction or TIA are lacking in China.

Therefore, the investigators conduct a multicenter cohort study to investigate the safety of early rivaroxaban in the AF patient with cerebral infarction or TIA within 12 days of onset.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

General Hospital of ShenYang Military Region

Shenyang, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Over 18 years
  • Acute cerebral infarction caused by non-valvular atrial fibrillation
  • NIHSS score ≤ 15
  • Within 12 days of onset
  • first stroke onset or past stroke without obvious neurological deficit (mRS score≤1)
  • Signed informed consent

Exclusion criteria

  • Hemorrhagic stroke or mixed stroke
  • Patients with valvular atrial fibrillation or non-cardiogenic cerebral infarction
  • Patients with severe infection or serious diseases
  • Gastrointestinal bleeding or major operation within 3 months
  • Planed cerebrovascular reconstruction or cardiac surgery within 3 months
  • Planed major surgery within 3 months
  • Participating in other clinical trials within 3 months
  • Unsuitable for this trial assessed by research

Treatment and study plan

Rivaroxaban

Drug

Rivaroxaban 15-20 mg daily

Primary outcomes

  1. incidence of intracranial hemorrhage

    Time frame: 7 days

Secondary outcomes

  1. incidence of early neurological deterioration

    Time frame: 7 days

    2 or more increase in NIHSS

  2. recurrence of stroke or other vascular events

    Time frame: 90 days

  3. bleeding event

    Time frame: 90 days

    Any bleeding event except intracranial hemorrhage

  4. Serious adverse events

    Time frame: 90 days

Sponsors and collaborators

Lead sponsor

General Hospital of Shenyang Military Region

Other

Registry information

Official study title

Early Rivaroxaban for Acute Ischemic Stroke or TIA Patients With Atrial Fibrillation: a Prospective, Multicenter, Cohort Study

Acronym: ERSAF

Important dates

Study start
2018
Primary completion
2025
Study completion
2025
First posted
Nov 21, 2018
Registry last updated
Aug 21, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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