CAPTURE - Complete Automatic Pacing Threshold Utilization Recorded by EnPulse

Completed · Not applicable

Conditions studied: Arrhythmia, Bradycardia

In brief

This study compares the pacemaker's automatic pacing threshold measurements to the manual measurements conducted by a health care provider.

Key facts

Study ID

NCT00275769

Run by

Medtronic Cardiac Rhythm and Heart Failure

People needed

860

Starts

2004-03-01

Expected to finish

2006-09-01

Last updated by the study team

2008-12-11

Who can join

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

You may qualify if…

• Patients that meet ACC/AHA/NASPE 2002 class I or II dual chamber pacing indications (intended for a Pacing Mode programmed to DDD or DDDR)

You may not qualify if…

• Patient with mechanical tricuspid heart valves
• Patients with medical conditions that preclude the testing required by the protocol or limit study participation

Where it is running

• Study site — Mobile, Alabama, United States
• Study site — Fullerton, California, United States
• Study site — Oceanside, California, United States
• Study site — Redondo Beach, California, United States
• Study site — Stanford, California, United States
• Study site — Colorado Springs, Colorado, United States
• Study site — Washington D.C., District of Columbia, United States
• Study site — Brandon, Florida, United States
• Study site — Daytona Beach, Florida, United States
• Study site — Orlando, Florida, United States
• Study site — Sarasota, Florida, United States
• Study site — Athens, Georgia, United States
• Study site — Gainsville, Georgia, United States
• Study site — Chicago, Illinois, United States
• Study site — Peoria, Illinois, United States
• Study site — Des Moines, Iowa, United States
• Study site — Kansas City, Kansas, United States
• Study site — Worcester, Maine, United States
• Study site — Burlington, Massachusetts, United States
• Study site — Petoskey, Michigan, United States
• Study site — Saint Paul, Minnesota, United States
• Study site — Jackson, Mississippi, United States
• Study site — Columbia, Missouri, United States
• Study site — St Louis, Missouri, United States
• Study site — Anchorage, Alabama, United States

Full record on ClinicalTrials.gov

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