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Real-time Continuous Cardiac Output Measurements

NCT ID: NCT04774978

Last Updated: 2021-03-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-03-01

Study Completion Date

2022-07-01

Brief Summary

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Study to assess the feasibility of real-time automatic cardiac output measurements using transthoracic echocardiography (TTE)

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Detailed Description

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Rationale: Study to assess the feasibility of real-time automatic cardiac output measurements using transthoracic echocardiography (TTE)

Objective: To assess the correlation and feasibility of real-time automatic continuous cardiac output measurements using transthoracic ultrasound (TTE) in adult ICU-patients in comparison to Flotrac measurements

Study design: prospective, feasibility study

Study population: Adult Intensive Care patients ( \> 18 years)

Intervention (if applicable):

Consecutive adult patients on the ICU in which the there is an indication for continuous cardiac output measurements.

Main study parameters/endpoints:

* Percentage of patients in which continuous cardiac output can be measured using TTE
* Correlation between continuous TTE and Flotrac measurements

Conditions

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Cardiac Output, Low

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Cardiac output measurements

Cardiac output will be measured using TTE continuously with ProbeFix

Group Type EXPERIMENTAL

TTE

Intervention Type DEVICE

Transthoracic echocardiography

Interventions

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TTE

Transthoracic echocardiography

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Adult Intensive Care patients ( \> 18 years)

Exclusion Criteria

* Pregnancy
* Atrial fibrillation or other irregular heart rhythm
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Rijnstate Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Central Contacts

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B Baten

Role: CONTACT

[email protected]
088 - 0057870

Other Identifiers

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RijnstateH

Identifier Type: -

Identifier Source: org_study_id

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