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Real-time Continuous Cardiac Output Measurements

R

Rijnstate Hospital

Status

Unknown

Conditions

Cardiac Output, Low

Treatments

Device: TTE

Study type

Interventional

Funder types

Other

Identifiers

NCT04774978
RijnstateH

Details and patient eligibility

About

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

Full description

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

Enrollment

20 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult Intensive Care patients ( > 18 years)

Exclusion criteria

  • Pregnancy
  • Atrial fibrillation or other irregular heart rhythm

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

Cardiac output measurements
Experimental group
Description:
Cardiac output will be measured using TTE continuously with ProbeFix
Treatment:
Device: TTE

Trial contacts and locations

0

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Central trial contact

B Baten

Data sourced from clinicaltrials.gov

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