Attain Success Clinical Trial

Completed

Conditions studied: Heart Failure

In brief

The purpose of the study is to assess lead implant success and complication rate using the Medtronic Attain Family of left-heart leads and delivery catheters.

Key facts

Study ID

NCT00990964

Run by

Medtronic Cardiac Rhythm and Heart Failure

People needed

2014

Starts

2009-11-01

Expected to finish

2011-11-01

Last updated by the study team

2012-09-12

Who can join

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

You may qualify if…

• Subject is at least 18 years of age or older
• Subject will be implanted with Medtronic cardiac resynchronization therapy (CRT) device and Medtronic left heart lead utilizing (or attempting to utilize) Attain Family of delivery catheters. The implant procedure may include upgrades to CRT from implantable pulse generator (IPG) or implantable cardioverter-defibrillator (ICD).

You may not qualify if…

• Subject is enrolled in a concurrent study with the exception of a study approved by the Medtronic Clinical Trial Leader prior to enrollment
• Subject has existing CRT system implanted or was previously implanted with a CRT system.

Where it is running

• Study site — Downey, California, United States
• Study site — Modesto, California, United States
• Study site — Redding, California, United States
• Study site — Riverside, California, United States
• Study site — San Diego, California, United States
• Study site — San Jose, California, United States
• Study site — Santa Rosa, California, United States
• Study site — Danbury, Connecticut, United States
• Study site — Washington D.C., District of Columbia, United States
• Study site — Delray Beach, Florida, United States
• Study site — Lake Mary, Florida, United States
• Study site — Naples, Florida, United States
• Study site — Orlando, Florida, United States
• Study site — Panama City, Florida, United States
• Study site — Saint Augustine, Florida, United States
• Study site — Tampa, Florida, United States
• Study site — Athens, Georgia, United States
• Study site — Atlanta, Georgia, United States
• Study site — Macon, Georgia, United States
• Study site — Marietta, Georgia, United States
• Study site — Chicago, Illinois, United States
• Study site — Decatur, Illinois, United States
• Study site — Indianapolis, Indiana, United States
• Study site — Newburgh, Indiana, United States
• Study site — Little Rock, Arkansas, United States

Full record on ClinicalTrials.gov

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