Trial Information
Summary: AN IMPORTANT CLINICAL TRIAL FOR ATRIAL FIBRILLATION
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NAVISTARŪ THERMOCOOLŪ Catheter for the Radiofrequency
Ablation of Symptomatic Paroxysmal Atrial Fibrillation
Overview:
Atrial fibrillation (AFib) is a rhythm disturbance of the heart
and the most common arrhythmia in clinical practice. The heart rate
of an AFib patient is between 300-600 beats per minute. An
individual who spontaneously alternates between AFib and a normal
heart rhythm is said to have paroxysmal atrial fibrillation (PAF).
PAF is often difficult to diagnose; some patients may be
asymptomatic while other patients may report symptoms such as
palpitations, fainting, and chest pain. In addition to potentially
life-altering symptomatic episodes, individuals with AFib have a
mortality rate that is twice as high as those with normal sinus
rhythm and have a risk of ischemic stroke between 2 and 7 times
that of those without AFib.1
Anti-arrhythmic drug therapy fails to control atrial
fibrillation (AFib) in many patients, who may also experience
intolerable side effects from their medications. In the past
decade, a number of catheter ablation approaches have been
investigated to treat AFib.
Catheter ablation is a procedure used to destroy (ablate) areas
of the heart muscle that are causing the arrhythmias. In a
radiofrequency (RF) catheter ablation procedure,
electrophysiologists pinpoint the area and then use radio wave
energy to cauterize the aberrant heart tissue causing the heart
rhythm abnormality. Ablation therapy is a treatment option for
patients who have not benefited from anti-arrhythmic drug (AAD)
therapy or do not tolerate the appropriate AAD therapy.
Antiarrhythmic drug therapy, the first choice of the AHA therapy
guidelines, fails to control AFib for one year in more than 50% of
individuals treated.1,2 Catheter RF Ablation is a relatively
non-invasive procedure that can, if successful, restore a normal
heart rhythm, and possibly eliminate the need for open-heart
surgery or long-term drug therapies. This clinical trial is
evaluating the safety and effectiveness of catheter ablation as a
treatment alternative to chronic drug therapy for PAF
patients.2
Purpose:
This trial compares the safety and effectiveness of catheter
ablation for PAF with antiarrhythmic drug therapy. The
investigational catheter being studied is the NAVISTARŪ THERMOCOOLŪ
irrigated-tip catheter. It is currently FDA-approved for commercial
distribution in the U.S. for treating patients with Type I atrial
flutter and drug refractory Ventricular Tachycardia for MI
patients. The catheter is approved for use in Europe for
endocardial ablation for treating cardiac arrhythmias.
Trial parameters:
This is a prospective, randomized, open-label, active-control
trial that will enroll up to 230 participants at up to 30 hospitals
in the U.S. Patients will be randomized using a 2:1 scheme for the
test procedure (ablation) and control (medical therapy) groups,
respectively. Patients who fail the trial medication may have an RF
ablation procedure according to protocol.
Eligibility:
Patients with symptomatic PAF who are 18 years and older will be
considered for the study.
Inclusion criteria:
- Paroxysmal AFib.
- 3 episodes in prior 6 months, one documented.
- Failure of at least one antiarrhythmic drug (class I or III, or
AV nodal blocking agents such as beta blockers, calcium channel
blockers) or intolerable side effects.
Please help advance the treatment of AFib. Refer
your eligible patients today.
Call 1-866-471-AFIB (2342) for more
information, or have your patient(s) contact the nearest site
listed
here.
Click here to fill out our online questionnaire to see if you
pre-qualify for participation. By answering these questions,
you are not obligated to participate in this study. The purpose of
these questions is only to determine if you might qualify. You are
free at any time to make a decision about your participation in
this process.
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Contact:
Coordinator: Young Park, R.N.
Good Samaritan Hospital
LA Cardiology
1245 Wilshire Blvd.
Suite 703 / Cardiology
Los Angeles, CA 90017
Telephone: 1-866-788-3933 (Call Center)
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Trial listings updated: June 1, 2008 at 6:32:35 AM