Combination Antithrombotic Treatment for Prevention of Recurrent Ischemic Stroke in IntraCranial Atherosclerotic diseaSe (CATIS- ICAS)

Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age40+
SponsorPopulation Health Research Institute

About this trial

CATIS-ICAS is a double-blind, randomized, placebo-controlled (RCT), phase III study seeking to demonstrate that oral rivaroxaban 2.5 mg twice daily plus aspirin daily is superior to clopidogrel 75 mg daily plus aspirin daily for 90 days followed by placebo plus aspirin daily for preventing recurrent stroke in those with ischemic stroke secondary to intracranial atherosclerotic disease (ICAD) of 30-99%, when started within 30 days of index stroke.

Eligibility criteria

Qualifiers

Age > 40 years

Ischemic stroke or high-risk TIA (motor and/ or speech involvement)

Randomization within 30 days of index stroke

Stroke potentially attributable to ICAS 30-99% (or flow gap on time-offlight MRA) of a major intracranial artery (internal carotid artery, middle cerebral artery, anterior cerebral artery, posterior cerebral artery, intracranial vertebral artery, or basilar artery) by MRA or CTA or catheter angiography.

Disqualifiers

Cardioembolic stroke

Indication for long-term dual antiplatelet or anticoagulant therapy (e.g. venous thromboembolism, coronary stent, mechanical prosthetic valve)

Intracranial arterial stenosis secondary to causes other than atherosclerosis e.g. dissection, moya moya disease

Substantial extracranial carotid artery disease ipsilateral to the qualifying stroke with plans for carotid revascularization

Trial design

Treatments tested in this trial

  • Rivaroxaban
  • ASA

Treatment groups

1,172 Participants
are divided into 2 treatment groups

Locations

This trial has no locations