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NCT04858126

Accuracy of ECOM Plus Versus Pulmonary Artery Catheter

Completed NA Last updated 20 February 2024
What this trial tests

NA trial testing ECOM cardiac output in Hemodynamic Monitoring in 110 participants. Completed in 11 September 2023.

Timeline
1 January 2021
Primary endpoint
11 September 2023
11 September 2023

Quick facts

Lead sponsorECOM Medical, Inc.
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposediagnostic
Enrollment110
Start date1 January 2021
Primary completion11 September 2023
Estimated completion11 September 2023
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

ECOM Medical, Inc.

Who can join

18 and older, any sex, with Hemodynamic Monitoring. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This Study will compare the accuracy of the ECOM Plus Endotracheal Cardiac Output Monitor (ECOM) without the use of the arterial pressure waveform from the arterial line to 1) the current clinical standard of cardiac output measured by intermittent room temperature bolus thermodilution using a PAC, 2) the current ECOM System with the use of the arterial blood pressure waveform from a radial arterial line and 3) the Flo-Trac® System.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Hemodynamic Monitoring

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04858126.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing