Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
160 participants
OBSERVATIONAL
2023-09-15
2025-04-30
Brief Summary
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Detailed Description
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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.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Derivation Sample
80 patients will be recruited as a derivation sample to calculate the regression equation
No interventions assigned to this group
Validation Sample
80 patients will be recruited as a validation sample to test the performance of the equation
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Sex: Both sexes.
* BMI: \<35
* Patient in whom central venous cannulation is needed for management.
* Spontaneously breathing patients.
Exclusion Criteria
* Patients who not able to lie supine.
* Patients on mechanical ventilation.
18 Years
ALL
No
Sponsors
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Ain Shams University
OTHER
Responsible Party
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Locations
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Department of Anesthesiology, Intensive Care, and Pain Management, Faculty of Medicine, Ain Shams University
Cairo, Cairo Governorate, Egypt
Countries
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Other Identifiers
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MD186/2023
Identifier Type: -
Identifier Source: org_study_id
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