NCT Number: NCT02331342
Comparison of NICOM and Innocor for Non-Invasive Determination of Cardiac Output
Cardiac output (CO) is an important parameter in the diagnosis and therapy of cardiac diseases. The aim of the study at hand was to evaluate NICOM (bioreactance) as a new method for determinion of CO and to compare it to Innocor (inert gas rebreathing), which previously showed promising results.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Observational
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- hemodynamic stability
- respiratory stability
Exclusion criteria
- patient unwilling to participate
Treatment and study plan
Innocor cardiac output measurement
DevicePrimary outcomes
-
Accuracy of NICOM and Innocor
Time frame: at time of inclusion
-
Precision of NICOM and Innocor
Time frame: at time of inclusion
Sponsors and collaborators
Lead sponsor
Universitätsmedizin Mannheim
Other
Registry information
Important dates
- Study start
- 2013
- Primary completion
- 2014
- Study completion
- 2014
- First posted
- Jan 6, 2015
- Registry last updated
- Jan 6, 2015
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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