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Evaluating the Fluid Balance of Mechanically Ventilated Patients by Ultrasonography

Measurement of the Inferior Vena Cava as a Method of Evaluating the Fluid Balance of Mechanically Ventilated Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03204292
Enrollment
57
Registered
2017-07-02
Start date
2015-07-31
Completion date
2017-01-31
Last updated
2017-07-02

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

Conditions

Fluid Loss, Fluid Overload

Keywords

Inferior vena cava, Fluid responsiveness, Central venous pressure

Brief summary

ratio of the diameter of inferior vena cava to the diameter of the thoracic aorta (IVC / Ao) depends on the daily balance of fluids.

Detailed description

During the routine abdominal ultrasound, the basilar and abdominal aorta were measured using a Sparq Philips ultrasonograph with a convex probe set in abdominal mode. All measurements were performed in one patient by the same operator who were experienced and performed the appropriate course of ultrasonography. The IVC and abdominal aorta were visualized using a paramedian long-axis view via a subcostal approach according to the methodology described by the American Society of Echocardiography. Inferior vena cava width was assessed at an interval of approximately 1 cm distal from connection of the hepatic vein to the inferior vena cava. No significant changes were observed in the width of the inferior vena cava during various respiratory phases, because of the positive pressure ventilation. The widest value was always chosen for the data. The assessment of the width of the abdominal aorta was performed above arise of the celiac trunk, at the height of the vein of the lower vena cava. The width of the inferior vena cava and the abdominal aorta was assessed using transthoracic ultrasound for the following five days. Daily differences in the amount of fluid intake and lost was recorded. CVP measurement was performed.

Interventions

None listed

Sponsors

Jagiellonian University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* patients who were hospitalized in the Intensive Care Unit * severe respiratory failure requiring mechanical ventilation

Exclusion criteria

* spontaneous breathing, * severe vascular disease, * increased intra-abdominal pressure, * cardiac pacemaker * cardioverter defibrillator

Design outcomes

Primary

MeasureTime frameDescription
fluid balance1 daythe width of the vena cava and abdominal aorta was measured every day morning. The difference in in taken and excreted fluids

Countries

Poland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026