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N/A Completed N=39 Single-blind Diagnostic

Clinical Evaluation of Cardiac Output Estimation Based on Pulse Wave Transit Time

Source: ClinicalTrials.gov NCT01877941 ↗
Enrolled (actual)
39
Serious AEs
0.0%
Results posted
Jan 2015
Primary outcomePrimary: esCCO (Estimated Continuous Cardiac Output) Monitor — 5.6 liters/minute

Summary

The specific aim of this study is to assess whether a device approved by the FDA to measure pulse oximetry can accurately estimate cardiac output.

Outcome Measures

OutcomeResultp-value
PRIMARY
esCCO (Estimated Continuous Cardiac Output) Monitor
5.6
PRIMARY
PAC (Pulmonary Artery Catheter).
4.95
PRIMARY
Cardiac Output as Measured by ECOM

Eligibility Criteria

Inclusion Criteria

  • Patients undergoing surgery where cardiac output will be measured with PAC and ECOM.

Exclusion Criteria

  • Failure to obtain consent.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01877941). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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