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Confirm Implantable Cardiac Monitor Study

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City:   Austin
State:   Texas
Zip Code:   78705
Conditions:   Tachyarrhythmias - Syncope
Purpose:   The goal of this IDE clinical study is to evaluate the quality of the cardiac signal recordings obtained by the SJM Confirm Implantable Cardiac Monitor (device).
Study Summary:  
Criteria:   Inclusion Criteria: - Patients who have clinical syndromes or situations at increased risk of cardiac arrhythmias - Patients who experience transient symptoms that may suggest a cardiac arrhythmia - Patients who have been previously diagnosed with atrial fibrillation - Patients who are suspected to have AF but AF has not been documented - Patients who have provided written informed consent to participate in the study. Exclusion Criteria: - Patients who are under the age of 18 years - Patients who have a life expectancy less than 1 year - Patients who are unable to comply with the follow-up schedule - Patients who are currently implanted with a pacemaker or defibrillator - Patients who the physician deems inappropriate for the study
NCT ID:   NCT00746564
Primary Contact:   Study Director
Tamara Shipman
St. Jude Medical

Tamara Shipman
Phone: 1-800-733-3455 ext. 6410
Email: tshipman@sjm.com
Backup Contact:   N/A
Location Contact:   Austin, Texas 78705
United States

Andrea Natale, MD
Phone: 512-458-1366

Site Status: Recruiting

Data Source:   ClinicalTrials.gov
Date Processed:   May 20, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
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