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Accuracy of IVCCI as a Measure of CVP

Accuracy of Inferior Vena Cava Collapsibility Index as a Measure of Central Venous Pressure

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06166875
Enrollment
160
Registered
2023-12-12
Start date
2023-12-15
Completion date
2025-04-30
Last updated
2026-05-28

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

Conditions

IVC Collapsibility Index

Brief summary

The primary aim of the current study is to examine the accuracy of IVCCI for measurement of CVP and to derive equation or formula to predict CVP from IVCCI.

Detailed description

Hemodynamic monitoring is important in the management of patients in the intensive care unit (ICU) Assessment of the intravascular volume, infusion of fluids or vasoactive drugs and maintenance of an adequate systemic perfusion is essential for reduction of the risk of organ failure and/or mortality. The use of CVP through central venous catheter is a gold standard method that is extensively used in the ICU as it reflects the filling pressure of the right ventricle (RV) and RV preload. Central venous cannulation has significant complications such as pneumothorax, hemothorax, arterial puncture, catheter malposition, cardiac arrhythmias, venous embolism, subcutaneous hematoma, and catheter related infection, and it is difficult to use this method in an emergency situation as it requires skilled personnel. Measurement of IVC index by bedside ultrasound is widely used to assess the intravascular volume in adult patients and has the advantage of being non-invasive, rapid, and reliable for assessing the volume status. Besides, related measures such as IVC diameter, IVC collapsibility, and IVC to aorta (AO) diameter have been applied clinically to assess the volume status and have been related to CVP.

Interventions

None listed

Sponsors

Nermeen Shawky Ahmed Mohamed
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Age: ≥18 years. * Sex: Both sexes. * BMI: \<35 * Patient in whom central venous cannulation is needed for management. * Spontaneously breathing patients.

Exclusion criteria

* Patients with increased intra abdominal pressure. * Patients who not able to lie supine. * Patients on mechanical ventilation.

Design outcomes

Primary

MeasureTime frame
The primary outcome of the current study is to examine the accuracy of IVCCI for measurement of CVP and to derive equation or formula to predict CVP from IVCCI.18 months

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 31, 2026