About this trial

A prospective, observational cohort study designed to identify clinical phenotypes and evaluate predictors \& outcomes of functional mitral and tricuspid valve regurgitation in patients with atrial fibrillation.

Participant will under go:

* Baseline echocardiography * Cpex Echocardiography * Blood test: BNP * 1 year follow up Echocardiography

Participants will be stratified into three subgroups:

* Atrial Functional MR * Atrial Functional TR * Mixed MR \& TR

Eligibility criteria

Qualifiers

Informed consent

Age of 18 years or older

Atrial fibrillation

Moderate or severe atrial valve disease

Disqualifiers

Unwilling or unable to give consent

Left ventricular impairment (ejection fraction < 50%).

Primary/organic valve disease

Trial design

Treatments tested in this trial

  • Echocardiogram

Treatment groups

No treatment groups listed

Locations

1
St Bartholomew's Hospital London United Kingdom

Sponsors and collaborators

Barts & The London NHS Trust

Lead sponsor