Combined Use of BIOTRONIK Home Monitoring and Predefined Anticoagulation to Reduce Stroke Risk

Stopped early · Phase 4

Conditions studied: Atrial Fibrillation, Atrial Flutter, Stroke, Embolism, Systemic Arterial, Major Bleeding

In brief

The IMPACT Study will investigate the potential clinical benefit of the combined use of BIOTRONIK Home Monitoring (HM) technology and a predefined anticoagulation plan compared to conventional device evaluation and physician-directed anticoagulation in patients with implanted dual-chamber defibrillators or cardiac resynchronization therapy devices.

Key facts

Study ID

NCT00559988

Run by

Biotronik, Inc.

People needed

2718

Starts

2008-02-01

Expected to finish

2013-06-01

Last updated by the study team

2017-12-05

Who can join

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

Where it is running

• Study site — Scottsdale, Arizona, United States
• Study site — Anaheim, California, United States
• Study site — Fremont, California, United States
• Study site — Santa Barbara, California, United States
• Study site — Torrance, California, United States
• Study site — Ventura, California, United States
• Study site — Aurora, Colorado, United States
• Study site — Boulder, Colorado, United States
• Study site — Newark, Delaware, United States
• Study site — Davenport, Florida, United States
• Study site — Daytona Beach, Florida, United States
• Study site — Kissimmee, Florida, United States
• Study site — Melbourne, Florida, United States
• Study site — Sarasota, Florida, United States
• Study site — St. Petersburg, Florida, United States
• Study site — Zephyrhills, Florida, United States
• Study site — Chicago, Illinois, United States
• Study site — Elk Grove Village, Illinois, United States
• Study site — Maywood, Illinois, United States
• Study site — Fort Wayne, Indiana, United States
• Study site — Valparaiso, Indiana, United States
• Study site — Shawnee Mission, Kansas, United States
• Study site — Lexington, Kentucky, United States
• Study site — Louisville, Kentucky, United States
• Study site — Phoenix, Arizona, United States

Full record on ClinicalTrials.gov

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