REGistry of Long-term AnTithrombotic TherApy-2

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorNational Medical Research Center for Cardiology, Ministry of Health of Russian Federation

About this trial

To assess the rates of ischemic and hemorrhagic complications of long-term antithrombotic therapy in patients with atrial fibrillation

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Documented atrial fibrillation with CHA2DS2VASC > 1

Disqualifiers

Subjects who are unwilling or unable to provide informed consent. ACS within 12 months before inclusion Severe CHF (NYHA IV) Stroke within 6 months before inclusion Severe liver or muscle disease Severe kidney disease / renal failure with creatinine > 3 mg/dl Conceivable impossibility to come in touch with the patient or his family at 1-year after the intervention

Trial population

Hospitalized or outpatients with confirmed atrial fibrillation and CHA2DS2VASC \> 1

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Anticoagulants

    Drug

    oral anticoagulants, dual or triple antithrombotic theraphy

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

composite of major cardiovascular events

stroke, myocardial infarction, stent thrombosis \[definite or probable\], or urgent revascularization, cqrdiac death

Time frame
unclusion up to 5 years
2

composite of any bleeding events

major, clinically relevant nonmajor, minor (BARC, ISTH,GARFIELD AF)

Time frame
unclusion up to 5 years

Secondary outcomes

1

Mutations in following genes

CYP2C9\*, VKORC1

Time frame
inclusion

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.