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CompletedPhase 2

Albumin for Management of Hypervolemic Hyponatremia (AlbuCAT)

Key facts

Who runs it
Fundacion Clinic per a la Recerca Biomédica
Where
Spain3 sites in 1 countryChoose a country to see its sites
Trial code
Status
Completed
Phase
Phase 2
People taking part
52 people enrolled
Started
1 Feb 2020
Ended
30 Jan 2025
Type of study
Interventional, 2 groupsOne group gets no study treatment, for comparison.
Treatments tested
  • Albumin treatment
Record updated
28 February 2025

Who can take part

Age
18 years and older
Sex
Women and men
Healthy volunteers
Cannot take part

The registry criteria, word for word

Show all 15 criteriaShow less

Who can take part

  • Patients included into the study must meet all the following criteria:; This study will include patients with liver cirrhosis and hypervolemic hyponatremia (serum sodium<130 mEq/L) admitted to hospital for any decompensation of the disease. Patients will be enrolled if hyponatremia persists after 3 days of diuretic withdrawal and fluid restriction. Women of child-bearing potential must have a negative pregnancy test in serum before the inclusion in the study and agree to use highly effective contraceptive methods, including intrauterine device, bilateral tubal occlusion or a vasectomized partner. Hormonal contraceptive methods will be avoided due to the risk of adverse events and impairment of liver function

Who cannot take part

  • Previous kidney or liver transplant
  • Severe alcoholic hepatitis defined by Maddrey score ≥32 and/or MELD score ≥ 20
  • Chronic kidney disease grade 3a or higher, defined as glomerular filtration rate <60ml/min for three months and markers of kidney damage (one or more): Albuminuria (Albumin excretion rate > 30 mg/24h; Albumin-to-creatinine ratio > 30 mg/g), Urine sediment abnormalities, Electrolyte and other abnormalities due to tubular disorders, Electrolyte and other abnormalities due to tubular disorders, Abnormalities detected by histology or Structural abnormalities detected by imaging
  • Active infection apart from spontaneous bacterial peritonytis based on positive culture (blood, urine, sputum or other samples) or by the following criteria:; Urinary infections: signs of systemic inflammation and more than 10 leukocytes per high-power field in urine; Pneumonia: compatible symptoms (cough, purulent sputum, chest pain, shortness of breath) and presence of new infiltrates on chest x-ray; Skin/soft tissue infection: physical exam findings of swelling, erythema, heat and tenderness in the skin; Acute cholangitis: signs of systemic inflammation1, compatible symptoms (right upper quadrant pain and jaundice) and radiological data of biliary obstruction, analytical data of cholestasis; Suspected bacterial infection: signs of systemic inflammation1 but no identifiable origin of this infection (polymorphonuclear cells in ascitic and pleural fluid < 250/mm3, normal urine sediment and chest Xray) After 48 hours of appropriate antibiotic treatment patients can be enrolled
  • Associated heart failure, defined as a New York Heart Association (NYHA) classification III or IV or heart failure with reduced ejection fraction (LVEF<40%). Previously known structural cardiomyopathy including ischemic cardiomyopathy, restrictive cardiomyopathy or valvular cardiomyopathy
  • Treatment with diuretics (furosemide or spironolactone), albumin infusion, somatostatin or terlipresin in the previous 3 days
  • Symptomatic hyponatremia (manifested by cardio-respiratory distress, abnormal and deep somnolence, seizures or coma) with serum sodium below 120 mEq/L
  • Previous known hypersensitivity to human albumin
  • Patients with Acute kidney injury 1B or higher
  • Spontaneous bacterial peritonitis
  • Hypo or hyperthyroidism not controlled under adequate treatment
  • Hepatocellular carcinoma beyond Milan criteria
  • ACLF with two or more organ failures
  • Refuse to give informed consent

This trial has no sites in United States.

It has sites in one country. Choose a country to see its sites.

About the trial

What the trial wants to find out

resolution of hyponatremia, defined as an increase in serum sodium of more than 5 mEq/L with a final value > 130 mEq/L, maintained for at least 48 consecutive hours during the 10-day treatment period

The 2 groups in the trial

  • No treatmentNo study treatment, for comparison
  • Albumin treatmentTreatment being tested

    one dose per day of a 40g albumin g/l gram(s)/litre for 10 days.

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Albumin for Management of Hypervolemic Hyponatremia in Patients With Decompensated Cirrhosis. A Proof of Concept Study.
Record updated
28 February 2025