Published: May 15, 2009
Medtronic Clinical Trial Evaluating the Newest Radiofrequency Ablation Tools for Atrial Fibrillation Completes Enrollment
MINNEAPOLIS - (BUSINESS WIRE) - Medtronic, Inc. (NYSE:MDT) today announced completion of enrollment in
the TTOP-AF (Tailored Treatment of Permanent Atrial Fibrillation)
clinical trial. The study is evaluating the use of the latest
radiofrequency (RF) ablation technology, the Medtronic Ablation
Frontiers Cardiac Ablation System, for the treatment of continuous
atrial fibrillation (AF). A leading advancement from currently available
RF ablation tools, the system is comprised of a RF generator (or energy
source) and three anatomically shaped mapping and ablation catheters
that target three areas of the heart for AF treatment. The system is
approved for use in Europe and is under investigational use in the
United States.
"Medtronic plans to be a leader in AF ablation by designing and
delivering breakthrough atrial fibrillation therapies to help physicians
treat the estimated seven million people worldwide suffering from this
disease," said Reggie Groves, vice president and general manager of
Medtronic's AF Solutions division. "Our goal is to provide safe, easy
solutions that offer more predictable procedure times than current
treatment methods and will allow physicians to customize care and reduce
the reoccurrence of AF for their patients."
The completion of enrollment follows Medtronic's recent acquisitions of
Ablation Frontiers, LLC, and CryoCath LP, to form Medtronic's AF
Solutions division. When combined with Medtronic's existing EP Systems
product portfolio, AF Solutions plans to offer a complete line of
diagnostic, cryoablation (freezing technology) and radiofrequency
ablation tools to treat the full range of AF patients.
"This unique system will offer physicians a way to tailor their care for
treating continuous atrial fibrillation in their patients," said John
Hummel, M.D., professor, Division of Cardiovascular Medicine at The Ohio
State University College of Medicine in Columbus, Ohio. "In this
clinical trial, the anatomical design of each catheter allowed me to
efficiently map and ablate broad areas in the left atrium. As a result,
the simplified process helped me decrease procedure times."
About the Medtronic Ablation Frontiers
Cardiac Ablation System
The Cardiac Ablation System is a minimally invasive catheter and
generator system that delivers customized radiofrequency energy designed
to eliminate or isolate abnormal electrical impulses in the left atrium
(upper left chamber of the heart) that initiate or sustain AF. The
three-dimensional, multi-electrode catheters are designed to allow
physicians to identify and selectively ablate a broader area of heart
tissue without the use of current single point catheters and complex
mapping and navigation equipment.
The Cardiac Ablation System includes:
-
Pulmonary Vein Ablation Catheter (PVAC) - designed for mapping,
ablating and verifying isolation of the pulmonary veins;
-
Multi-Array Septal Catheter (MASC) - designed for mapping and
ablating the left atrial septal wall;
-
Multi-Array Ablation Catheter (MAAC) - designed for mapping and
ablating the left atrial body; and
-
GENius Multi-Channel Radiofrequency Generator - the unique RF energy
delivery system allows physicians to tailor the location, depth and
fill of each ablation lesion.
About TTOP-AF
This pivotal trial is studying the safety and efficacy of the Cardiac
Ablation System in continuous AF patients. Patients were randomized to
receive ablation therapy or receive commonly used drug treatments. For
every three patients enrolled, approximately two received an ablation
and one was randomly assigned to the drug therapy group. The trial
allowed patients in the drug therapy group to receive an ablation if
they did not respond to drug therapy. Twenty-four centers enrolled 209
patients who will be followed for at least six months after the ablation
procedure. Upon trial completion, results will be submitted in
consideration for U.S. Food and Drug Administration (FDA) approval for
the Medtronic Ablation Frontiers Cardiac Ablation System.
About Atrial Fibrillation
Atrial fibrillation (AF or A Fib) is an irregular quivering or rapid
heart rhythm in the upper chambers (atria) of the heart. AF is the most
common cardiac rhythm condition, found in approximately three million
Americans and seven million people worldwide.¹ Untreated AF patients
have a two to seven times higher risk of stroke.2 Atrial
fibrillation causes inefficient pumping of the heart and can lead to
other rhythm problems including chronic fatigue and congestive heart
failure. Half of AF patients who receive treatment are non-responsive to
drug therapy, making them potential candidates for ablation therapy.
¹Millenium Research Report; "Global Markets For Atrial Fibrillation
Treatment Devices 2008," March 2008; 1.
2 T. Fetsch, EHJ.
2004;1385-1394.
About Medtronic
Medtronic, Inc. (www.medtronic.com),
headquartered in Minneapolis, is the global leader in medical technology
- alleviating pain, restoring health, and extending life for millions of
people around the world.
Any forward-looking statements are subject to risks and uncertainties
such as those described in Medtronic's Annual Report on Form 10-K for
the year ended April 25, 2008. Actual results may differ materially from
anticipated results.
Medtronic, Inc.
Catherine Peloquin, 763-526-2494
Public
Relations (U.S.)
Jeff Warren, 763-505-2696
Investor Relations
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