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Albumin for Management of Hypervolemic Hyponatremia (AlbuCAT) (AlbuCAT)

Primary Purpose

Hyponatremia With Excess Extracellular Fluid Volume, Cirrhosis, Liver

Status
Unknown status
Phase
Phase 2
Locations
Spain
Study Type
Interventional
Intervention
Albumin treatment
Sponsored by
Fundacion Clinic per a la Recerca Biomédica
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hyponatremia With Excess Extracellular Fluid Volume

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 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.

Exclusion Criteria:

  1. Patients with Acute kidney injury 1B or higher;
  2. 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.
  3. Previous kidney or liver transplant;
  4. Active infection apart from spontaneous bacterial peritonytis based on positive culture (blood, urine, sputum or other samples) or by the following criteria:

    1. Urinary infections: signs of systemic inflammation and more than 10 leukocytes per high-power field in urine;
    2. Pneumonia: compatible symptoms (cough, purulent sputum, chest pain, shortness of breath) and presence of new infiltrates on chest x-ray;
    3. Skin/soft tissue infection: physical exam findings of swelling, erythema, heat and tenderness in the skin;
    4. Acute cholangitis: signs of systemic inflammation1, compatible symptoms (right upper quadrant pain and jaundice) and radiological data of biliary obstruction, analytical data of cholestasis;
    5. 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.
  5. Spontaneous bacterial peritonitis.
  6. Hypo or hyperthyroidism not controlled under adequate treatment.
  7. 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.
  8. Hepatocellular carcinoma beyond Milan criteria.
  9. Severe alcoholic hepatitis defined by Maddrey score ≥32 and/or MELD score ≥ 20
  10. ACLF with two or more organ failures
  11. Treatment with diuretics (furosemide or spironolactone), albumin infusion, somatostatin or terlipresin in the previous 3 days.
  12. Symptomatic hyponatremia (manifested by cardio-respiratory distress, abnormal and deep somnolence, seizures or coma) with serum sodium below 120 mEq/L.
  13. Previous known hypersensitivity to human albumin
  14. Refuse to give informed consent

Sites / Locations

  • Hospital Clinic de Barcelona
  • Hospital Moises Broggi
  • Hospital Parc Taulí

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

No treatment

Albumin treatment

Arm Description

No treatment.

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

Outcomes

Primary Outcome Measures

Resolution of hyponatremia
defined as an increase in serum sodium of more than 5 mEq/L with a final value > 130 mEq/L

Secondary Outcome Measures

partial resolution of hyponatremia
defined as an increase in serum sodium of more than 5meq/L with a final value below 130meq/L,
Evaluation of systemic hemodynamics
mean arterial pressure
kidney function
measurement of creatinine levels
Effects on the inflammatory profile
evaluation of PCR of plasma cytokines by using a multiplex kit including plasmatic cytokines related to immune response. This multiplex test will be performed at day 0 and day 10 of the study period (or at the end of study in case of early termination).
Effects on neurocognitive function and quality
PHES questionnaire
Effects on brain water content
performance of aMagnetic Resonance Spectroscopy (MRS)
Effects of albumin administration on liver phagocytic capacity
Effects of albumin administration on liver phagocytic capacity as assessed by performance of hepatic SPECT with 99mTc-phytate at day 0 and 10 (or at the end of study in case of early termination).
Effects on phagocytic capacity and inflammatory response of peripheral monocytes
Effects on phagocytic capacity and inflammatory response of peripheral monocytes will be assessed by performance specific tests (Phagotest and Phagoburst) evaluating the in vitro phagocytic capacity and burst response. Monocytes will be isolated and analysed at day 0 and at day 10 of the study period (or at the end of study in case of early termination).
Effects of albumin administration of microbiome composition
Effects of albumin administration of microbiome composition as assessed by analysis of microbiome composition at day 0 and 10 of the study period (or at the end of study in case of early termination).
Effects of albumin administration on development of infections, development of complications of cirrhosis and survival.
Effects of albumin administration on development of infections, development of complications of cirrhosis and survival.
Effects of albumin administration on serum albumin levels
Effects of albumin administration on serum albumin levels assessed by measurement of mEq/L serum albumin levels at day 0, 5, 10, 28 and 90 of study period.
evaluate treatment-related serious adverse events
To evaluate treatment-related serious adverse events during the treatment period

Full Information

First Posted
March 28, 2019
Last Updated
February 4, 2020
Sponsor
Fundacion Clinic per a la Recerca Biomédica
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1. Study Identification

Unique Protocol Identification Number
NCT03941405
Brief Title
Albumin for Management of Hypervolemic Hyponatremia (AlbuCAT)
Acronym
AlbuCAT
Official Title
Albumin for Management of Hypervolemic Hyponatremia in Patients With Decompensated Cirrhosis. A Proof of Concept Study.
Study Type
Interventional

2. Study Status

Record Verification Date
February 2020
Overall Recruitment Status
Unknown status
Study Start Date
July 2020 (Anticipated)
Primary Completion Date
July 2022 (Anticipated)
Study Completion Date
November 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fundacion Clinic per a la Recerca Biomédica

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hyponatremia With Excess Extracellular Fluid Volume, Cirrhosis, Liver

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
52 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
No treatment
Arm Type
No Intervention
Arm Description
No treatment.
Arm Title
Albumin treatment
Arm Type
Experimental
Arm Description
one dose per day of a 40g albumin g/l gram(s)/litre for 10 days.
Intervention Type
Drug
Intervention Name(s)
Albumin treatment
Other Intervention Name(s)
Human Albumin Grifols 200 g/l, solution for infusion
Intervention Description
one dose per day of a 40g albumin g/l gram(s)/litre for 10 days. 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
Primary Outcome Measure Information:
Title
Resolution of hyponatremia
Description
defined as an increase in serum sodium of more than 5 mEq/L with a final value > 130 mEq/L
Time Frame
for at least 48 consecutive hours during the 10-day treatment
Secondary Outcome Measure Information:
Title
partial resolution of hyponatremia
Description
defined as an increase in serum sodium of more than 5meq/L with a final value below 130meq/L,
Time Frame
maintained for at least 48 consecutive hours during the 10-day treatment period.
Title
Evaluation of systemic hemodynamics
Description
mean arterial pressure
Time Frame
levels at day 0, at day 5 and at day 10 (or at the end of study in case of early termination due to primary endpoint reach from day 0 up to 10 days) of the study period.
Title
kidney function
Description
measurement of creatinine levels
Time Frame
levels at day 0, 5 and 10 (or at the end of study in case of early termination due to primary endpoint reach from day 0 up to 10 days).
Title
Effects on the inflammatory profile
Description
evaluation of PCR of plasma cytokines by using a multiplex kit including plasmatic cytokines related to immune response. This multiplex test will be performed at day 0 and day 10 of the study period (or at the end of study in case of early termination).
Time Frame
levels at day 0, and 10 (or at the end of study in case of early termination due to primary endpoint reach from day 0 up to 10 days).
Title
Effects on neurocognitive function and quality
Description
PHES questionnaire
Time Frame
levels at day 0, and 10 (or at the end of study in case of early termination due to primary endpoint reach from day 0 up to 10 days).
Title
Effects on brain water content
Description
performance of aMagnetic Resonance Spectroscopy (MRS)
Time Frame
levels at day 0, and 10 (or at the end of study in case of early termination due to primary endpoint reach from day 0 up to 10 days).
Title
Effects of albumin administration on liver phagocytic capacity
Description
Effects of albumin administration on liver phagocytic capacity as assessed by performance of hepatic SPECT with 99mTc-phytate at day 0 and 10 (or at the end of study in case of early termination).
Time Frame
levels at day 0, and 10 (or at the end of study in case of early termination due to primary endpoint reach from day 0 up to 10 days).
Title
Effects on phagocytic capacity and inflammatory response of peripheral monocytes
Description
Effects on phagocytic capacity and inflammatory response of peripheral monocytes will be assessed by performance specific tests (Phagotest and Phagoburst) evaluating the in vitro phagocytic capacity and burst response. Monocytes will be isolated and analysed at day 0 and at day 10 of the study period (or at the end of study in case of early termination).
Time Frame
levels at day 0, and 10 (or at the end of study in case of early termination due to primary endpoint reach from day 0 up to 10 days).
Title
Effects of albumin administration of microbiome composition
Description
Effects of albumin administration of microbiome composition as assessed by analysis of microbiome composition at day 0 and 10 of the study period (or at the end of study in case of early termination).
Time Frame
levels at day 0, and 10 (or at the end of study in case of early termination due to primary endpoint reach from day 0 up to 10 days).
Title
Effects of albumin administration on development of infections, development of complications of cirrhosis and survival.
Description
Effects of albumin administration on development of infections, development of complications of cirrhosis and survival.
Time Frame
levels at day 0, and 10 (or at the end of study in case of early termination due to primary endpoint reach from day 0 up to 10 days).
Title
Effects of albumin administration on serum albumin levels
Description
Effects of albumin administration on serum albumin levels assessed by measurement of mEq/L serum albumin levels at day 0, 5, 10, 28 and 90 of study period.
Time Frame
levels at day 0, 5, 10, 28 and 90 of study period.
Title
evaluate treatment-related serious adverse events
Description
To evaluate treatment-related serious adverse events during the treatment period
Time Frame
visit day 1,2,3,4,5,6,7,8,9,28 and 90

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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. Exclusion Criteria: Patients with Acute kidney injury 1B or higher; 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. Previous kidney or liver transplant; 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. Spontaneous bacterial peritonitis. Hypo or hyperthyroidism not controlled under adequate treatment. 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. Hepatocellular carcinoma beyond Milan criteria. Severe alcoholic hepatitis defined by Maddrey score ≥32 and/or MELD score ≥ 20 ACLF with two or more organ failures 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 Refuse to give informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Anna Cruceta
Phone
0034 93 2279838
Email
acruceta@clinic.ub.es
Facility Information:
Facility Name
Hospital Clinic de Barcelona
City
Barcelona
State/Province
Catalunya
ZIP/Postal Code
08036
Country
Spain
Facility Name
Hospital Moises Broggi
City
Barcelona
State/Province
Catalunya
Country
Spain
Facility Name
Hospital Parc Taulí
City
Sabadell
State/Province
Catalunya
ZIP/Postal Code
08208
Country
Spain

12. IPD Sharing Statement

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Albumin for Management of Hypervolemic Hyponatremia (AlbuCAT)

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