Medtronic Shock-Less Study on Physician Utilization of Shock Reduction Programming

Completed

Conditions studied: Cardiovascular Disease

In brief

The purpose of this clinical trial is to determine whether periodic therapy programming reports illustrating physician usage of shock reduction programming can increase utilization of recommended programming guidelines for defibrillators.

Key facts

Study ID

NCT00856349

Run by

Medtronic Cardiac Rhythm and Heart Failure

People needed

4384

Starts

2009-04-01

Expected to finish

2013-03-01

Last updated by the study team

2014-07-03

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subject (or subject's legally authorized representative) is willing and able to sign and date the Patient Consent Form (PCF) and authorization for access to and use of health information, if applicable
• Subject has been implanted with a Medtronic market released ICD or CRT-D device (US/Canada - Concerto®/Virtuoso® or newer model; AsiaPacific, Israel, Latin America - EnTrust™, InSync Sentry®, or Concerto®/Virtuoso® or newer model) within the past 30 days
• Subject has commercially released RA (if applicable), RV, and LV (if applicable) leads

You may not qualify if…

• Subject is enrolled in a concurrent study that has not been approved for concurrent enrollment by the Medtronic Clinical Trial Leader

Where it is running

• Study site — Phoenix, Arizona, United States
• Study site — Tucson, Arizona, United States
• Study site — Hot Springs, Arkansas, United States
• Study site — Little Rock, Arkansas, United States
• Study site — Fremont, California, United States
• Study site — Fresno, California, United States
• Study site — Modesto, California, United States
• Study site — Northridge, California, United States
• Study site — Orange, California, United States
• Study site — San Bernardino/Los Angeles, California, United States
• Study site — Ventura, California, United States
• Study site — New Haven, Connecticut, United States
• Study site — Fort Lauderdale, Florida, United States
• Study site — Jacksonville, Florida, United States
• Study site — Ocala, Florida, United States
• Study site — Palm Beach Gardens, Florida, United States
• Study site — Pensacola, Florida, United States
• Study site — Plantation, Florida, United States
• Study site — Rockledge, Florida, United States
• Study site — St. Petersburg, Florida, United States
• Study site — Zephyrhills, Florida, United States
• Study site — Atlanta, Georgia, United States
• Study site — Berwyn, Illinois, United States
• Study site — Elk Grove Village, Illinois, United States
• Study site — Anniston, Alabama, United States

Full record on ClinicalTrials.gov

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