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Fluid Challenge Impact in the Portal Vein Pulsatility Depending on the Fluid Responsivness Status (FLUID-REVENGE)

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Civil Hospices of Lyon

Status

Completed

Conditions

Cardiovascular Insufficiency
Venous Congestion

Study type

Observational

Funder types

Other

Identifiers

NCT05828407
2023-A00196-39 (Other Identifier)
69HCL22_1115

Details and patient eligibility

About

Portal vein pulsatility index is a marker of venous congestion evaluated by point of care ultrasound. It is associated with acute kidney injury, especially in critically ill patients. It may be considered as a dynamic marker. The investigators hypothesized that portal vein pulsatility index is higher after a fluid challenge only in patient without preload dependence in critically ill patients with cardiovascular insufficiency.

Enrollment

36 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • vasopressor requirement to maintain mean arterial pressure >65mmHg AND

  • at least one of the following criteria:

    • arterial lactate >2mmol/L;
    • capillary refill time >3s;
    • mottling score >1;
    • diuresis <0,5mL/h for more than 6hours.

Exclusion criteria

  • Diameter of vena cava <20mm
  • Cirrhosis
  • Pregnancy
  • Severe acute pulmonary edema
  • Phototype 4 or 5
  • Patient opposition to participate

Trial design

36 participants in 1 patient group

Cohort
Description:
Population: Critically ill patient with: * cardio circulatory insufficiency as defined by vasopressor requirement and at least one of the following criteria: arterial lactate \>2mmol/L ; capillary refill time \>3s ; mottling score \>1 ; diuresis \<0,5mL/h for more than 6hours * diameter of inferior vena cava \>20mm Protocol: Administration of a fluid challenge (4mL/kg of Ringer Lactate) over 5 to 10 min. Point of care ultrasound evaluation of portal vein pulsatility index and Vexus criteria before and after the fluid challenge ; fluid challenge induced cardiac index variations estimated by pulse contour analysis

Trial contacts and locations

1

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Central trial contact

Martin RUSTE, MD

Data sourced from clinicaltrials.gov

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