The purpose of the study is to assess combining AF ablation, with AV node ablation and
pacemaker implantation for patients suffering with 'irregular heartbeats' or atrial
fibrillation. The study will last 13 months.
Procedure: AF ablation and AV node ablation
Procedure: AV node ablation
We will connect you to the doctor responsible for this trial and help you get more information.
Locations near you
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Full eligibility criteria for NCT01057485
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Patients with symptomatic drug refractory atrial fibrillation.
Patients who have had pacemaker implantation and AV node ablation with ongoing symptoms.
Patients will already be refractory to at least 2 rate or rhythm control drugs.
Patients must be over 18 years old.
Patients give informed consent form prior to participating in this study.
Patient is suffering with unstable angina in last 1 week.
Patient has had a myocardial infarction within last 2 months.
Patient is expecting or has had major cardiac surgery within last 2 months.
Patient is participating in a conflicting study.
Patient is unable to perform exercise testing.
Patient is mentally incapacitated and cannot consent or comply with follow-up.
Patient has NYHA class III/ IV heart failure.
Patient has LVEF <35% not secondary to tachycardia.
Patient suffers with other cardiac rhythm disorders.
Recent coronary artery intervention or other factors suggesting clinical instability
(ECG, clinical or laboratory findings).
All locations for NCT01057485
United Kingdom (1)
Eastbourne District General Hospital
Eastbourne, East Sussex, United Kingdom, BN21 2UD
Put me in touch!
View full eligibility
Tris trial is registered with FDA with number: NCT01057485. The sponsor of the trial is Eastbourne General Hospital and it is looking for 50 volunteers for the current phase.
Official trial title: Node and Atrial Fibrillation Ablation for Persistent Atrial Fibrillation
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