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Accuracy of IVCCI as a Measure of CVP

A

Ain Shams University

Status

Completed

Conditions

IVC Collapsibility Index

Study type

Observational

Funder types

Other

Identifiers

NCT06166875
MD186/2023

Details and patient eligibility

About

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.

Full 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.

Enrollment

160 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

160 participants in 2 patient groups

Derivation Sample
Description:
80 patients will be recruited as a derivation sample to calculate the regression equation
Validation Sample
Description:
80 patients will be recruited as a validation sample to test the performance of the equation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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