Comparison of a Novel 12-Lead Wireless Electrocardiogram (ECG) and a Standard Wired ECG
NCT ID: NCT00998842
Last Updated: 2009-11-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
10 participants
OBSERVATIONAL
2009-10-31
2009-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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healthy subjects
five male, five female, ages 18-64
Recom Model 100
Battery Operated, Ambulatory, Digital Wireless ECG Monitor System
GE 5000 ECG Monitor System
Wired ECG system
Interventions
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Recom Model 100
Battery Operated, Ambulatory, Digital Wireless ECG Monitor System
GE 5000 ECG Monitor System
Wired ECG system
Eligibility Criteria
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Inclusion Criteria
* Age 18-64
Exclusion Criteria
* Prisoners,
* Have known cardiovascular disease, OR
* Do not pass the PAR-Q and/or show baseline ECG abnormalities.
18 Years
64 Years
ALL
Yes
Sponsors
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Oklahoma State University Center for Health Sciences
OTHER
University of Oklahoma
OTHER
Responsible Party
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University of Oklahoma
Locations
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Family Medicine Clinic
Tulsa, Oklahoma, United States
Countries
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Other Identifiers
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OU IRB 14853
Identifier Type: -
Identifier Source: org_study_id
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