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
49 participants
OBSERVATIONAL
2011-10-31
2013-05-31
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
Eligibility Criteria
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Inclusion Criteria
* male and female patients aged at least 18 years
Exclusion Criteria
* implanted pacemaker / CRT / ICD exept Medtronic OptiVol
* patients being unable to consent
18 Years
90 Years
ALL
No
Sponsors
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RWTH Aachen University
OTHER
Responsible Party
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Locations
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Univeristy Hospital Aachen
Aachen, North Rhine Westfalia, Germany
Countries
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Other Identifiers
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10-081
Identifier Type: -
Identifier Source: org_study_id
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