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OpenTrials
Completed

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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Key information

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

NICOM cardiac output measurement

Device

Innocor cardiac output measurement

Device

Primary outcomes

  1. Accuracy of NICOM and Innocor

    Time frame: at time of inclusion

  2. 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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