Early treatment of atrial fibrillation for stroke prevention trial (EAST – AFNET 4)

Atrial fibrillation is by far the most common cardiac arrhythmia and affects approx. 1 to 2 percent of the European population. Atrial fibrillation is indeed not immediately life-threatening, but it can have serious consequences. So, patients with atrial fibrillation have a fivefold higher risk of having a stroke.

With the treatment options available so far, i.e., especially with blood thinners and with rate control for atrial fibrillations, these serious consequences of atrial fibrillation can only be partially prevented.

The possibilities of rhythm control treatment of atrial fibrillation have significantly broadened in recent years: The so-called catheter ablation of atrial fibrillation has been an established procedure to prevent in particular early forms of atrial fibrillation (paroxysmal, non-persistent atrial fibrillation) for some years.

In the EAST – AFNET 4 study, atrial fibrillation shall be detected early on. Patients who are diagnosed with atrial fibrillation for the first time or patients who have suffered from atrial fibrillation for less than 1 year will be randomised into a group with early rhythm control care or a group with the usual care.

Patients in the early care group will be treated corresponding to the current ESC guidelines for the treatment of atrial fibrillation. They will also undergo a catheter ablation or will receive an antiarrhythmic therapy.

The patients in the usual care group will be treated with the treatment measures usually used nowadays in accordance with the guidelines (anticoagulation, rate control).

The aim of the EAST- AFNET 4 study is to investigate whether early, comprehensive rhythm control treatment of atrial fibrillation using safe antiarrhythmic agents and catheter ablation is suitable to prevent cardiovascular complications associated with long-term atrial fibrillation.

This is a phase IV study in accordance with the Medicinal Products Act (AMG). The study will be conducted at over 160 sites in 11 European countries. All patients will be monitored up to 2 years after the end of the study within the scope of follow-up visits.

The AFNET study has been partially funded by the DZHK from 2015 to 2020.

EAST-AFNET 4 Homepage

Publications

Check out all publications of EAST-AFNET 4.

Principal Investigators

Paulus Kirchhof (Birmingham, Münster)

Study information
EAST – AFNET 4

Recruiting status
Study completed
Recruitment start
07.2011
Patients
2789
2789
Clinical Trials Registrierung

NCT01288352

Category
Guideline relevant study
Links
http://www.easttrial.org/

Operative contact: Heidi Oellers
(Heidi.oellers@af-net.eu)