ClinicalTrials.Veeva

Menu

Inferior Vena CAVA and Lung UltraSound-guided Therapy in Acute Heart Failure (CAVAL US-AHF)

I

Instituto Cardiovascular de Buenos Aires

Status

Completed

Conditions

Acute Heart Failure
Heart Failure

Treatments

Other: Standard of care
Other: CAVAL US-guided Therapy

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Between 25% and 30% of patients hospitalized for acute heart failure (AHF) are readmitted within 90 days after discharge. Mostly due to persistent congestion on discharge. However, as the optimal evaluation of decongestion is not clearly defined, it is necessary to implement new tools to identify subclinical congestion to guide treatment.

Enrollment

60 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Hospitalization of 24 hours or greater for decompensated heart failure defined as new-onset of symptoms or worsening of previous symptoms (including orthopnea, progression to FC III-IV, bendopnea or fatigue) or signs of volume overload.

and - Jugular venous distension, hepatojugular reflux, lower extremity edema or signs of pulmonary congestion.

and

  • Chest X-ray with signs suggestive of pulmonary congestion. and
  • Elevated ´pro-B-type natriuretic peptide (NT-proBNP) levels of 450 pg/mL, 900 pg/mL, and 1800 pg/mL for ages < 50 years, 50 to 75 years, and > 75 years, respectively, within 24 hours of admission (53,54).

and

  • Sufficient ultrasound visualization to assess IVC and lungs.

Exclusion criteria

  • Not willing to participate.
  • Life expectancy of less than 6 months.
  • Uninterpretable lung or inferior vena cava ultrasound.
  • Transfer to another hospital before hospital discharge.
  • SBP < 90 mm Hg.
  • Chronic kidney disease (creatinine clearance <30 mL/min calculated with the MDRD equation or hemodialysis).
  • Requirement for invasive or noninvasive ventilator support.
  • Pregnancy.
  • Low cardiac output syndrome/cardiogenic shock.
  • Death during index hospitalization.
  • Acute coronary syndrome, myocardial revascularization or heart valve replacement within the previous 3 months.
  • Being on heart transplant waiting list.
  • Cardiac resynchronization therapy device implanted within the previous 3 months.
  • Severe tricuspid valve regurgitation.
  • Heart failure secondary to causes amenable to invasive correction: cardiac surgery, percutaneous interventions or pacemaker implantation.
  • Heart failure secondary to significant arrhythmias (advanced atrioventricular block or sinus arrest, sustained ventricular tachycardia or any sustained arrhythmia other than atrial fibrillation causing hemodynamic instability according to the discretion of the treating physician).
  • Heart failure secondary to severe systemic infection
  • Severe psychiatric illness
  • Palliative care
  • SARS-CoV-2 infection

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

60 participants in 2 patient groups

CAVAL US group
Experimental group
Description:
Patients assigned to this group will receive a daily CAVAL US exam guided decongestive therapy accessible to the treating medical team, in addition to standard care. Diuretic titration: There will not be a specific treatment protocol, but clinicians will be encouraged to tailor treatment, particularly with the use of diuretics, according to the number of B-lines and dilation in the IVC. The therapeutic objective will be discharge patients normal CAVAL US, with relief of congestive signs and symptoms of HF, without electrocardiographic or laboratory alterations that contraindicate discharge.
Treatment:
Other: Standard of care
Other: CAVAL US-guided Therapy
Standard of care group
Active Comparator group
Description:
Patients assigned to this group will receive standard care, and diuretic titration will be based on standard practice (physical examination, symptoms, and laboratory results). The therapeutic objective will be discharge patients with relief of congestive signs and symptoms of HF, without electrocardiographic or laboratory abnormalities that contraindicate discharge.
Treatment:
Other: Standard of care

Trial contacts and locations

2

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems