Apixaban for the Reduction of Thrombo-Embolism in Patients With Device-Detected Sub-Clinical Atrial Fibrillation

Completed · Phase 4

Conditions studied: Atrial Fibrillation, Stroke

In brief

This study aims to determine if treatment with apixaban, compared with aspirin, will reduce the risk of ischemic stroke and systemic embolism in patients with device-detected sub-clinical atrial fibrillation and additional risk factors for stroke.

Key facts

Study ID

NCT01938248

Run by

Population Health Research Institute

People needed

4012

Starts

2015-05-01

Expected to finish

2023-11-03

Last updated by the study team

2023-11-15

Who can join

Age: 55 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Permanent pacemaker or defibrillator (with or without resynchronization) or insertable cardiac monitor capable of detecting SCAF
• At least one episode of SCAF ≥ 6 minutes in duration but no single episode > 24 hours in duration at any time prior to enrollment. Any atrial high rate episode with average > 175 beats/min will be considered as SCAF. No distinction will be made between atrial fibrillation and atrial flutter. SCAF requires electrogram confirmation (at least one episode) unless ≥ 6 hours in duration.
• Age ≥ 55 years
• Risk Factor(s) for Stroke:
• Previous stroke, TIA or systemic arterial embolism OR Age at least 75 OR Age 65-74 with at least 2 other risk factors OR Age 55-64 with at least 3 other risk factors
• Other risk factors are:
• hypertension
• CHF
• diabetes
• vascular disease (i.e. CAD, PAD or Aortic Plaque)
• female

You may not qualify if…

• Clinical atrial fibrillation documented by surface ECG (12 lead ECG, Telemetry, Holter) lasting ≥ 6 minutes, with or without clinical symptoms
• Mechanical valve prosthesis, deep vein thrombosis, recent pulmonary embolism or other condition requiring treatment with an anticoagulant
• Contra-indication to apixaban or aspirin:
• Allergy to aspirin or apixaban
• Severe renal insufficiency (creatinine clearance must be calculated in all patients; any patient with either a serum creatinine > 2.5 mg/dL [221 µmol/L] or a calculated creatinine clearance < 25 ml/min is excluded)
• Serious bleeding in the last 6 months or at high risk of bleeding (this includes, but is not limited to: prior intracranial hemorrhage, active peptic ulcer disease, platelet count < 50,000/mm3 or hemoglobin < 10 g/dL, recent stroke within past 10 days, documented hemorrhagic tendencies or blood dyscrasias)
• Moderate to severe hepatic impairment
• Ongoing need for combination therapy with aspirin and clopidogrel (or other combination of two platelet inhibitors)
• Meets criteria for requiring lower dose of apixaban AND also has ongoing need for strong inhibitors of CYP 3A4 or P-glycoprotein (e.g., ketoconazole, itraconazole, ritonavir or clarithromycin)
• Ongoing need for strong dual inducers of CYP 3A4 or P-glycoprotein (e.g., rifampin, carbamazepine, phenytoin, St. John's wort)
• Received an investigational drug in the past 30 days
• Participants considered by the investigator to be unsuitable for the study for any of the following reasons:
• Not agreeable for treatment with either aspirin or apixaban or anticipated to have poor compliance on study drug treatment
• Unwilling to attend study follow-up visits
• Life expectancy less than the expected duration of the trial2 years due to concomitant disease
• Women who are pregnant, breast-feeding or of child-bearing potential without an acceptable form of contraception in place (sterilization, hormonal contraceptives, intrauterine device, barrier methods or abstinence)

Where it is running

• St. Vincent Heart Clinic — Little Rock, Arkansas, United States
• Cardiovascular Associates of Marin and San Francisco Medical — Larkspur, California, United States
• Aurora Denver Cardiology Associates — Aurora, Colorado, United States
• Naples Interventional Cardiac Electrophysiology — Naples, Florida, United States
• Langhorne Cardiology Consultants, Inc. — Pensacola, Florida, United States
• One Health Cardiology, Owensboro Health, Inc. — Owensboro, Kentucky, United States
• Tufts Medical Center — Boston, Massachusetts, United States
• Sparrow Clinical Research Institute — Lansing, Michigan, United States
• Michigan Heart — Ypsilanti, Michigan, United States
• University of Missouri Health System — Columbia, Missouri, United States
• St. Louis Heart and Vascular — St Louis, Missouri, United States
• Glacier View Cardiology — Kalispell, Montana, United States
• The Cooper Health System — Camden, New Jersey, United States
• Hackensack University Medical Center — Hackensack, New Jersey, United States
• The Valley Hospital — Ridgewood, New Jersey, United States
• St. Peter's Health Partners Medical Association, PC — Albany, New York, United States
• Carolinas Healthcare System — Charlotte, North Carolina, United States
• WakeMed — Raleigh, North Carolina, United States
• Cleveland Clinic — Cleveland, Ohio, United States
• Pennsylvania State University — Hershey, Pennsylvania, United States
• Research Institute of LG Health / Penn Medicine — Lancaster, Pennsylvania, United States
• Virginia Heart — Falls Church, Virginia, United States
• Onze Lieve Vrouw Ziekenhuis — Aalst, Belgium
• Vivalia CSL St. Joseph — Arlon, Belgium
• Cardiovascular Associates of Mesa, PC — Mesa, Arizona, United States

Full record on ClinicalTrials.gov

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