Prediction and monitoring of cardiac response to intravenous fluid administration by non-invasive measurement of the initial systolic time interval after cardiac surgery

Prediction and monitoring of cardiac response to intravenous fluid administration by non-invasive measurement of the initial systolic time interval after cardiac surgery - Cardiac fluid response and ISTI measurement

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON33850

Enrollment

Registered

2009-07-09

Start date

2009-08-09

Completion date

Unknown

Last updated

2024-05-06

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

Conditions

coronary artery disease heart monitoring

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Intensive-care patients who are presumably hypovolaemic and who have a clinical reason for fluid administration.

Exclusion criteria

Exclusion criteria: Younger than 18 or older than 80 years of age; medical, practical or ethical drawbacks or objections to participate. Blood loss by bleeding at a rate of over 100 ml/h. Relevant alterations in inotropic and vasopressor medication.

Design outcomes

Primary

Measure	Time frame
The study parameters are: PEP and the respiratory change delta-PEP, ISTI and delta-ISTI and cardiac output CO.	—

Secondary

Measure	Time frame
None	—

Countries

Netherlands

Outcome results