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Caval Aorta Index for Fluid Optimization in Traumatic Brain Injury

Efficacy of Caval Aorta Index for Fluid Optimization in Critically Ill Patients With Traumatic Brain Injury

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06940258
Acronym
CAI for fluids
Enrollment
92
Registered
2025-04-23
Start date
2025-05-01
Completion date
2026-07-31
Last updated
2025-04-29

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

Conditions

Fluid Balance

Keywords

caval aorta index, traumatic brain injury

Brief summary

Traumatic brain injury is a leading cause of death and disability in trauma patients. As the primary injury cannot be reversed; management strategies must focus on preventing secondary injury by avoiding hypotension and hypoxia besides, maintaining appropriate cerebral perfusion pressure, which is a surrogate for cerebral blood flow.

Detailed description

The caval aorta index is an ultrasound element, relatively new, used to assess volume status. Technically, the sonographic assessment of the inferior vena cava /aorta diameter ratio is an easy test to perform and can be performed effectively by doctors who are not experienced in the field of sonography (Kusumastuti et al .2021). In this study; the caval aorta index will be used to guide fluid dosage in critically ill patients with traumatic brain injury.

Interventions

PROCEDUREultrasound measurement of caval aorta index

ultrasound measurement of caval aorta index

OTHERcontrol group

fixed fluid prescription

Sponsors

Mansoura University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Masking description

A vascular US expert will read the number contained in computer generated randomization software and determine group assignments. Daily; he will be responsible on prescribing of the required fluid.

Intervention model description

After enrollment, patients will be randomly allocated using block into two groups of 46 patients in each group; ultrasound-guided fluid management (US group) or standard care (C group)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

Traumatic brain injury diagnosed by computed tomography scan Glasgow coma score ≥ 4

Exclusion criteria

Inability to get consent. Pregnant and lactating women Traumatic subarachnoid hemorrhage Spinal cord injury Increased intra-abdominal pressure Abdominal aortic aneurysm Inferior vena cava (IVC) thrombus Portal hypertension Acute corpulmonale Congestive heart failure chronic hemodialysis Surgical intervention other than neurological one within the first 7 days Mechanical ventilation need during first 7 days Cardiac arrest during the first 7 days

Design outcomes

Primary

MeasureTime frameDescription
fluid balanceafter 96 hours from the admissionthe difference between fluid input and fluid loss

Secondary

MeasureTime frameDescription
Central Venous Pressure (CVP) measurementsDaily every 6 hours for 7 dayscm H2O
Frequency and duration of hypotensionwithin first 7 dayssystolic blood pressure less than 90 mmhg
Urine outputDaily for 7 weeksmL
Central capillary refillDaily for 7 daysseconds
incidence of pulmonary edemaDaily within first 7 daysnew B-lines in lung Ultrasound
Glasgow Coma Scaledaily within first 7 daysrange from 3-to-15

Contacts

Primary ContactMaha Ahmed Abozeid, Assistant Professor
mahazed@yahoo.com02-01019216192

Outcome results

None listed

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