Aortic blood flow velocity variation as a predictor of fluid responsiveness in patients during coronary artery bypass surgery

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00009632

Enrollment

Registered

2016-01-05

Start date

2015-05-01

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

Fluid Responsiveness

Interventions

Group 1: Comparison of the stroke volume variation (SVV) and the pulse pressure variation (PPV) derived by pulse contour analysis with the variations of the blood flow velocity in the LVOT and the aor

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Adult patients who were scheduled for coronary artery bypass grafting

Exclusion criteria

Exclusion criteria: Permanent absence of cardiac sinus rhythm (i.e. atrial fibrillation), highly impaired left and/or right ventricular function (ejection fraction <30%). mid- or high grade valve stenosis and/or insufficieny. Contraindications to transesophageal echocardiography.

Design outcomes

Primary

Measure	Time frame
The primary goal of this study is to proof that the parameters measured by echocardiography to describe the fluid responsiveness are comparable to the paramters derived by pulse contour analysis.	—

Secondary

Measure	Time frame
The secondary goal of this study is to show that the cardiac output measured by echocardiography is comparable to the cardiac output measured by pulse contour analysis.	—

Countries

Germany

Contacts

Public ContactAdrian Stephan

Universitätsklinikum Heidelberg

adrian.stephan@med.uni-heidelberg.de062215636107

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026