Frontlight ResearchEarly access
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