1204 Participants NeededMy employer runs this trial

Edoxaban + Antiplatelet Therapy for Stroke Prevention

(STROKE75+ Trial)

DG
Overseen ByDavid Gladstone, BSc, MD, PhD, FRCPC
Age: 65+
Sex: Any
Trial Phase: Phase 3
Sponsor: Sunnybrook Health Sciences Centre
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Pivotal Trial (Near Approval)This treatment is in the last trial phase before FDA approval
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

The overall aim of this research is to improve secondary stroke prevention for older patients with stroke.

In current practice, patients with stroke are often prescribed antiplatelet therapy with either aspirin or clopidogrel to help prevent recurrent strokes. However, an antiplatelet medication may not be effective enough for some patients.

A promising new treatment strategy to enhance stroke prevention involves a very low dose of an anticoagulant (anti-clotting medication) added to the standard antiplatelet therapy. In a previous study, this approach cut stroke risk in half among patients with heart/vascular disease, but it has not yet been formally tested in an older stroke population. The STROKE75+ trial is now being conducted to carefully evaluate the potential benefits and potential risks of this type of treatment strategy for secondary stroke prevention.

The medication being tested in the STROKE75+ trial is a commonly used anticoagulant called edoxaban -- at a reduced dose of 15mg once daily (one-quarter of its full dose) to minimize the chance of bleeding. In previous research, edoxaban 15mg daily has been shown to be safe and effective for preventing strokes in patients with atrial fibrillation, but it has not been studied in stroke patients without atrial fibrillation.

This trial aims to answer the following questions:

1. Does the addition of edoxaban 15mg once a day to standard antiplatelet therapy reduce the risk of recurrent strokes more than standard antiplatelet therapy alone?

2. Does the addition of edoxaban 15mg daily reduce the risk of severe (disabling) strokes, dementia, or heart attacks?

3. What is the incidence of bleeding with/without edoxaban 15mg daily?

These questions will be addressed using a Randomized Clinical Trial design. Eligible participants are randomly assigned (50/50 chance) to one of two study groups. Participants in Group 1 are treated with edoxaban 15 mg once a day by mouth (tablet) in addition to their usual standard antiplatelet medication. Participants in Group 2 will continue to take their standard antiplatelet medication (aspirin or clopidogrel) without edoxaban.

Participants are monitored closely for the duration of the study (approx.. 2-4 years). Every 3 months, participants will receive a phone call to check on their health status and assess if they have experienced any new strokes, bleeding, or other medical problems. Once a year, and at the start and end of the study, participants will also be asked questions about their symptoms, functioning, memory, and quality of life. At the end of the study, patient outcomes between the two groups will be compared and the results will be published.

The information gained from this study will increase knowledge and help inform future stroke care for the aging population. The ultimate goal of this research is to prevent more strokes, save lives, and reduce the growing public health burden of stroke.

Are You a Good Fit for This Trial?

This trial is for people aged 75 or older who have had an ischemic stroke (or certain types of mini-strokes) in the past year, confirmed by brain scan. They must be taking aspirin or clopidogrel to prevent another stroke and not have a history of atrial fibrillation on heart monitoring.

Inclusion Criteria

4. Written informed consent from participant or legally authorized representative.
3. The patient has had ECG monitoring after the qualifying stroke event (Holter, telemetry, or other continuous ECG monitoring device) totalling at least 24 hours and with no episodes of atrial fibrillation (or atrial flutter) ≥6 minutes AND a routine 12-lead ECG within 90 days before randomization shows sinus rhythm (no atrial fibrillation or atrial flutter).
I am 75 years old or older.
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What Are the Treatments Tested in This Trial?

Interventions

  • Aspirin
  • Clopidogrel
  • Edoxaban 15 mg

Trial Overview

The study compares two groups: one takes a low dose of edoxaban (an anticoagulant) plus their usual antiplatelet medicine (aspirin or clopidogrel), while the other continues with just their standard antiplatelet medicine. Participants are randomly assigned and followed for about 2-4 years.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: Intervention Group (combination therapy group)Experimental Treatment2 Interventions
Group II: Control Group (standard-care group)Active Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Sunnybrook Health Sciences Centre

Lead Sponsor

Trials
693
Recruited
1,569,000+