NCT Number: NCT00294034
VIBRANT Registry: Value of Information Based From Pacemaker Recordings and New Technologies
The purpose of this study is to collect data from pacemakers and determine how this information is used by physicians to care for their patients with pacemakers.
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Conditions
Sex eligibility
All sexes
Study type
Observational
Primary location
Hot Springs, Arkansas, United States
About this study
The purpose of this registry is to gain a better understanding of how diagnostic capabilities in four Vitatron pacemakers (Selection AFm, Clarity, C-Series, and T-Series) are being utilized for the clinical management of a general pacing population. Pacemaker information and health status is collected from all patients enrolled.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Class I or Class II indication for dual chamber pacing
Exclusion criteria
- Has an ICD or is a known candidate for an ICD
Treatment and study plan
Sponsors and collaborators
Lead sponsor
Medtronic Cardiac Rhythm and Heart Failure
Industry
Collaborators
- Medtronic
- Medtronic BRC
Registry information
Important dates
- Study start
- 2002
- Study completion
- 2006
- First posted
- Feb 20, 2006
- Registry last updated
- Mar 27, 2007
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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