- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00295204
Evaluation of a Mobile Cardiac Outpatient Telemetry System Versus Standard Loop Event Monitor
Evaluation of a Mobile Cardiac Outpatient Telemetry System (CardioNet) Versus Standard Loop Event Monitor: A Multi-Center Randomized Study
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment
Contacts and Locations
Study Locations
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New Jersey
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Bridgewater, New Jersey, United States, 08807
- Medicor Cardiology, PA
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Elizabeth, New Jersey, United States, 07202
- Garden State Cardiovascular Associates
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Ocean, New Jersey, United States, 07712
- Monmouth Cardiology Associates, LLC
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New York
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Flushing, New York, United States, 11355
- Cardiovascular Associates of NY
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Pennsylvania
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Abington, Pennsylvania, United States, 19001
- Abington Medical Specialists
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Doylestown, Pennsylvania, United States, 18901
- Central Bucks Cardiology
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Doylestown, Pennsylvania, United States, 18901
- Central Bucks Specialitsts, LTD
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Jenkintown, Pennsylvania, United States, 19046
- PA Heart and Vascular Group
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Lancaster, Pennsylvania, United States, 17603
- Lancaster Heart and Stroke Foundation
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Pittsburgh, Pennsylvania, United States, 15219
- Southwestern PA Cardiology Associates
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Pottstown, Pennsylvania, United States, 19464
- Pottstown Medical Specialistsq
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Yardley, Pennsylvania, United States, 19067
- Cardiology Consultants of Phladelphia
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Virginia
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Richmond, Virginia, United States, 23226
- Virginia Cardiovascular Specialist
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- syncope, pre-syncope or palpitations less frequently than every 24 hours Pre-syncope without loss of consciousness defined as transient dizziness, leghtheadedness, unsteadiness or weak spells: syncopal events with or without warning: palpitations Subjects with non-diagnostic 24 hours of monitoring related to symptoms within 45 days of enrollment into study Subject able to understand, assent to , and willing to sign the Informed Consent Form.
Exclusion Criteria:
- Class IV heart failure Post Myocardial infarction less than or equal to 3 months Unstable angina defined as chest pain at rest, new onset of angina, or a change in existing patterns of angina.
Subjects who are candidatees for or have had recent (less than or equal to 3 monthr) heart valve surgery History of sustained ventricualr tachycardia or ventricular fibrillation documented EF 35% or less with complex ectopy defined as PVC's 10 or greater per hour.
Subject is less than 18 years old at the time of signing informed consent. Any condition which may prohibit the completion of or compliance with the protocol.
Study Plan
How is the study designed?
Design Details
- Time Perspectives: Other
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Stephen Rothman, MD, Mainline Arrhythmia and Cardiology Associates
Study record dates
Study Major Dates
Study Start
Study Completion
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 05-002
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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