Confirm Implantable Cardiac Monitor Study

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:		Charlottesville, Virginia 22980 United States *There is no listed contact information for this specific location.* Site Status: Completed

Data Source:		ClinicalTrials.gov
Date Processed:		May 24, 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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