Comparison of NICOM and Innocor for Non-Invasive Determination of Cardiac Output

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02331342

Enrollment

Registered

2015-01-06

Start date

2013-07-31

Completion date

2014-06-30

Last updated

2015-01-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Disease

Keywords

Agreement of NICOM and Innocor

Brief summary

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.

Interventions

DEVICENICOM cardiac output measurement

DEVICEInnocor cardiac output measurement

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

* hemodynamic stability * respiratory stability

Exclusion criteria

* patient unwilling to participate

Design outcomes

Primary

Measure	Time frame
Accuracy of NICOM and Innocor	at time of inclusion
Precision of NICOM and Innocor	at time of inclusion

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026