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CompletedNCT06254703VExLUS-KRTUpdated May 8, 2026

Venous Excess and Lung Ultrasound During Continuous Kidney Replacement Therapy in Critically Ill Patients

An observational study in Acute Kidney Failure Stage 3, sponsored by Chulalongkorn University. Completed at 1 site in Thailand. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-05-08.

Sponsored by Chulalongkorn University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
100
Ages
18 Years and older
Sex
All
01

Study summary

Hemodynamic management of critically ill patients has long been focused on the arterial side of the vasculature by assessing adequate perfusion pressure. However, the venous pressure is also of critical importance. Venous congestion can occur in patients with right ventricular failure, pulmonary hypertension or fluid overload. Fluid overload has harmful effects to end organs causing acute kidney injury (AKI), lung edema, multiorgan dysfunction and death. Vice versa, AKI can aggravate fluid retention and inflammation. The measurement of venous pressure usually relies on central venous pressure (CVP) and inferior vena cava diameter (IVC). However, CVP measurement has been associated with measurement errors and has low accuracy in predicting fluid responsiveness. Moreover, IVC collapsibility or distensibility is a static parameter and is associated with subjective variability.

Multiorgan Point-of-Care ultrasound (POCUS) can enhance the management of AKI by enabling the evaluation of renal structural abnormalities and hemodynamic status . POCUS allows the clinician to assess intravascular and pulmonary fluid overload. It has been shown that POCUS is a good parameter to predict global fluid status of the patient .

Venous Excess Ultrasound (VEXUS) consists of the evaluation of IVC, hepatic vein, portal vein and intrarenal vein flow pattern. Previous studies showed significant correlation between VExUS score with RRT-free days and guide fluid management in critically ill patients with AKI . VExUS is useful in predicting patients at risk to develop AKI post cardiac surgery . Adding modified lung ultrasound score to the VExUS protocol could help clinician to adjust fluid administration and achieve proper fluid balance during continuous kidney replacement therapy (CKRT). However, the role of using combined VExUS and lung ultrasound in the assessment and guidance of fluid management during CKRT is unknown.

Read the detailed description

Lung and cardiac ultrasonography can augment the definite diagnosis of volume overload. Thoracic ultrasound demonstrating B-lines which suggest thickened interstitial or fluid filled alveoli or increased vena cava diameter by ultrasound can also be used to assess volume status.

Recently, the venous excess ultrasound grading system (VExUS) has been introduced to be used in conjunction with POCUS to assess significant congestion. This technique used to classify the level of venous congestion by assessing the abdominal blood flow, including hepatic veins (HVs), portal veins (PVs) and intrarenal veins (IRVs). Abnormal patterns of flow in these organs can enhance the clinical evaluation of venous congestion in addition to Inferior vena cava (IVC) ultrasound since organ dysfunction occurring with venous congestion can also be from the transmission of pressure from right atrium (right atrial pressure, RAP) to the peripheral organ. Venous congestion is classified into four grades , ranging from grade 0 (no congestion) to the most severe form, grade 3 (severe congestion) or VExUS "A" through "E".

In the Modified VExUS score, the VExUS grade 0 by IVC cut-off by ≤ 2 cm is replaced with the IVC distensibility index \< 18% or the IVC collapsibility index \< 50%, depending on patient passive or active ventilation, respectively.

Lung ultrasound and AKI Volume overload is associated with interstitial edema which increases the diffusion distance for oxygen and induces an increase in interstitial fluid pressure, impairing capillary blood flow and exacerbating organ dysfunction . A prospective pilot observational study with 45 adult patients with AKI at any time during ICU stay employed the FALLS (Fluid Administration Limited by Lung Ultrasound) protocol in which they use the LUS for assessing volume status. A new onset of the B-lines was considered as the endpoint of fluid administration. The study demonstrated a linear correlation between baseline B-line scores and PaO2/FiO2 ratio in ICU patients VExUS and lung ultrasound during CKRT

Previous studies have shown that VExUS and lung ultrasound may play a role in predicting AKI severity and may aid fluid de-escalation in critically ill patients. However, no studies have evaluated the role of both VExUS, modified VExUS and lung ultrasound in guiding fluid management during CKRT. Our research aims to evaluate the prevalence of venous congestion by VExUS, mVExUS and lung ultrasound during CKRT and its association with clinical outcomes.

02

Conditions studied

  • Acute Kidney Failure Stage 3

Keywords

  • Acute kidney injury
  • VexLUS
  • Critically ill
  • Kidney replacement therapy
  • Continuous kidney replacement therapy
  • POCUS
  • modifiedVExUS
03

In context

Acute Kidney Injury

1,594 studies on the registry are indexed under Acute Kidney Injury; 370 are open to participants now.

This study's enrollment of 100 is below the median of 151 across 772 observational studies indexed under Acute Kidney Injury.

Browse Acute Kidney Injury studies →

Lead sponsor

Chulalongkorn University is the lead sponsor of 312 studies on the registry; 59 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

patients without ESRD that initiate CKRT

Inclusion criteria

  1. Adults (≥ 18 years of age)
  2. Admitted to ICU
  3. Plan to initiate CKRT by clinician's judgement

Exclusion criteria

Exclusion Criteria:

  1. Refuse to participate
  2. Previous diagnosis of end-stage kidney disease (ESKD) currently on kidney replacement therapy
  3. Kidney tran splant recipient
  4. Receive KRT before ICU admission
  5. Structural kidney diseases which will interfere with intrarenal doppler ultrasound e.g. renal artery stenosis, autosomal dominant polycystic kidney disease etc.
  6. Patients with previously known conditions that interfere with portal doppler assessment, namely liver cirrhosis, severe tricuspid regurgitation with structural heart disease or massive ascites.
  7. Underlying disease process with a life expectancy less than 90 days
  8. Pregnancy
  9. Concomitant severe respiratory distress syndrome
  10. Expected life expectancy \<48 hours
  11. Receiving extracorporeal membrane oxygenation (ECMO)
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
100 participants (actual)
Patient registry
No

Groups and cohorts

  • Patients receiving CKRT

    1. Adults (≥ 18 years of age) 2. Admitted to ICU 3. Plan to initiate CKRT by clinician's judgement

    Diagnostic Test: VExUS (venous excess ultrasound) · Diagnostic Test: modified VExUS (modified venous excess ultrasound)

Interventions

  • Diagnostic testVExUS (venous excess ultrasound)

    IVC, hepatic veins (HVs), portal veins (PVs) and intrarenal veins (IRVs), and lung ultrasound

    Also known as: Bioelectrical impedence (BIA), N-terminal pro B-type natriuretic peptide (NT-proBNP), modifiedVExUS

  • Diagnostic testmodified VExUS (modified venous excess ultrasound)

    replace the IVC maximal diameter cut-off by ≤ 2 cm with the IVC distensibility index \< 18% or the IVC collapsibility index \< 50%, depending on patient passive or active ventilation, respectively.

06

What researchers measure

Primary outcomes

  1. To assess the prevalence of venous congestion by using VExLUS and modifiedVExUS in patients who receive CKRT

    prevalence of venous congestion

    Time frame: 1 day

Secondary outcomes

  1. To evaluate the association between VExLUS and modifiedVExUS scores and all-cause mortality within 90 days, KRT-free days, ventilator-free days, vasopressor-free days, ICU-free days, dialysis dependence ay 28 days and 90 days

    clinical outcomes

    Time frame: up to 90 days

  2. - to assess the correlation of VExLUS and modifiedVExUS score with bioelectrical impedance vector analysis (BIVA) parameters and biomarkers

    Correlation to BIVA

    Time frame: 1 day

  3. to evaluate inter-observer variability in determining VExLUS

    inter-observer variability

    Time frame: 3 days

  4. To evaluate the association between VExLUS and modifiedVExUS scores and all-cause mortality within 28 days

    28 days all cause mortality

    Time frame: 28 days

  5. Association between protein-calorie malnutrition and mortality in patients with acute kidney injury (AKI) undergoing continuous renal replacement therapy (CRRT).

    To determine the association between protein-calorie malnutrition and mortality in patients with acute kidney injury (AKI) undergoing continuous renal replacement therapy (CRRT).

    Time frame: 7 days after enrollment

  6. optimal protein and energy supplementation and mortality

    To identify the optimal amount of protein and energy supplementation required to reduce mortality.

    Time frame: From enrollment to the end of treatment at 28 days

  7. Maximum level of protein and energy intake association with clinical outcomes

    To determine the maximum levels of protein and energy intake associated with the best clinical outcomes.

    Time frame: from enrollment upto 28 days

  8. Current prescribed protein and energy in AKI patients during CRRT

    To find the current prescribed protein and energy practice in AKI patients during CRRT?

    Time frame: from enrollment date to 7 days after enrollment

  9. association between energy intake, protein intake and nPCR in AKI patients during CRRT

    To find association between energy intake, protein intake and nPCR in AKI patients during CRRT with clinical outcomes.

    Time frame: from enrollment to 7 days after enrollment

  10. correlation between protein intake and nPCR

    To find the correlation between prescribed protein intake and nPCR?

    Time frame: from enrollment to 7 days after enrollment

07

Study locations

1 site
  • King chula memorial hospital
    Bangkok, Bangkok 10330, Thailand
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 8, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06254703
Lead sponsor
Chulalongkorn University
Responsible party
Nuttha Lumlertgul, MD (Principal investigator, Chulalongkorn University) — Principal investigator
First posted
Feb 12, 2024
Start date
Mar 1, 2024
Primary completion
Nov 20, 2025
Completion
Nov 30, 2025
Last update
May 8, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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