Attain Model 4196 Left Ventricular (LV) Lead

Completed · Not applicable

Conditions studied: Heart Failure

In brief

Heart failure is a progressive disease that decreases the pumping action of the heart. This may cause a backup of fluid in the heart and may result in heart beat changes. When there are changes in the heart beat sometimes an implantable heart device is used to control the rate and rhythm of the heart beat. In certain heart failure cases, when the two lower chambers of the heart no longer beat in a coordinated manner, cardiac resynchronization therapy (CRT) may be prescribed. CRT is similar to a pacemaker. It is placed (implanted) under the skin of the upper chest. CRT is delivered as tiny electrical pulses to the right and left ventricles through three or four leads (flexible insulated wires) that are inserted through the veins to the heart. The purpose of this study is to evaluate a new lead for delivering energy to the left ventricle (bottom left chamber of the heart).

Key facts

Study ID

NCT00271544

Run by

Medtronic Cardiac Rhythm and Heart Failure

People needed

190

Starts

2007-02-01

Expected to finish

2008-12-01

Last updated by the study team

2009-09-28

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• QRS greater than or equal to 120 milliseconds (The QRS interval is a measurement of how the electrical signal involved in a heart beat travels, or is conducted, through the ventricles. A wide QRS (more than 120) suggests that there is a conduction problem, or block, in the ventricles.)
• Left Ventricular Ejection Fraction (EF) less than or equal to 35 percent (Ejection Fraction is a measurement of how well the left ventricle pumps blood out to the rest of the body. The higher the EF the more blood the ventricle is pumping.)
• Subject has moderate to severe heart failure despite medications

You may not qualify if…

• Subjects with a previous lead in the left ventricle or previous implant attempt within 30 days of implant or ongoing complications from a previous unsuccessful attempt
• Subjects with chest pain or who have had a heart attack within the past month before enrollment in the study
• Subjects that have had certain surgeries on their heart within the past three months
• Subjects with chronic (permanent) fast heart beats in the upper chambers of the heart (atrial arrhythmias)

Where it is running

• Study site — Anchorage, Alaska, United States
• Study site — Phoenix, Arizona, United States
• Study site — Long Beach, California, United States
• Study site — Palo Alto, California, United States
• Study site — Davenport, Iowa, United States
• Study site — Lexington, Kentucky, United States
• Study site — Baton Rouge, Louisiana, United States
• Study site — Detroit, Michigan, United States
• Study site — Minneapolis, Minnesota, United States
• Study site — Kansas City, Missouri, United States
• Study site — Raleigh, North Carolina, United States
• Study site — Mayfield Heights, Ohio, United States
• Study site — Wynnewood, Pennsylvania, United States
• Study site — Spartanburg, South Carolina, United States
• Study site — Kingsport, Tennessee, United States
• Study site — Memphis, Tennessee, United States
• Study site — Dallas, Texas, United States
• Study site — Fort Worth, Texas, United States
• Study site — Burlington, Vermont, United States
• Study site — Calgary, Alberta, Canada
• Study site — Edmonton, Alberta, Canada
• Study site — Toronto, Ontario, Canada
• Study site — Montreal, Quebec, Canada
• Study site — Sainte-Foy, Quebec, Canada

Full record on ClinicalTrials.gov

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