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Effects of Maintaining Steady Albumin Levels (TAT 4) on Survival and Liver Related Complications in Cirrhosis With Ascites

Primary Purpose

Liver Cirrhosis

Status
Unknown status
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
ALB Protein, Human
placebo
Sponsored by
Institute of Liver and Biliary Sciences, India
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Liver Cirrhosis

Eligibility Criteria

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

Inclusion Criteria:

  • Newly detected cirrhotic patients aged more than 18 years
  • Cirrhosis defined by standard clinical, analytical and/or histological criteria
  • Serum albumin level < 2.8g/dl with or without ascites
  • Who would agree to give written informed consent

Exclusion Criteria:

  • Uncontrolled HTN (sys>150/ dis >90 mmHg) or h/o any drug therapy for HTN
  • Prior h/o Transjugular Intrahepatic Portosystemic Shunt (TIPS)
  • Hepatocellular Carcinoma
  • Active alcohol abuse within 3 months
  • Patients presenting as Acute on Chronic Liver Failure
  • Extrahepatic organ failure
  • Known case of chronic heart failure or respiratory failure
  • Diagnosed Chronic Kidney Disease
  • Patients with hydrothorax
  • Prior liver transplant recipient
  • Human Immunodeficiency Virus infection
  • Use of albumin infusion in the last one month
  • CTP>12, MELD>28
  • Total Bilirubin >3 g/dl
  • Overt Hepatic Encephalopathy at Presentation

Sites / Locations

  • Institute of Liver & Biliary SciencesRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Albumin

Placebo

Arm Description

Albumin infusions will be given at a dose of 40 g twice weekly till a steady albumin level of 4.0g/dl is reached followed by 100ml of 20% albumin at least once in two weeks to maintain a steady albumin level of 4.0g/dl along with the standard medical therapy

Placebo

Outcomes

Primary Outcome Measures

Transplant/Transintrahepatic Portosystemic Shunt (TIPS) free survival in both groups
1 year survival

Secondary Outcome Measures

New onset refractory ascites in both the groups
refractory ascites is defined as non response to maximum tolerated dose of diuretics
Spontaneous bacterial peritonitis [SBP] in both groups
Spontaneous bacterial peritonitis is defined as ascitic fluid absolute neutrophil count > 250/ mL with or without culture positivity
Renal impairment in both groups
serum creatinine concentration >1•5 mg/dL
Hepatorenal Syndrome in both groups
Hepatorenal Syndrome type 1 is defined as new onset increase in serum creatinine level by 0.3 mg/dL or 50% increase from baseline
Hepatic encephalopathy grade 3 or 4 in both groups
HE as per West Haven criteria
Number of new cases with gastrointestinal bleeding in both groups
gastrointestinal bleeding as confirmed by endoscopic/clinical evidence of variceal bleed.
Requirement of paracentesis in both groups
Ascitic tapping for relieve of pressure symptoms or diagnosis of SBP
Requirement of diuretics in both groups
Frusemide or Aldactone for management of ascites
Number of hospitalizations per subject in both groups
Need for any cause hospitalization
New onset breathlessness/ Hypertension within 24 hours of albumin infusion in both groups
Development of cardiac overload
Quality of life by Ascite-Q questionnaire in both groups
semiquantitative questionnaire to be answered by the participants

Full Information

First Posted
August 13, 2019
Last Updated
September 11, 2019
Sponsor
Institute of Liver and Biliary Sciences, India
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1. Study Identification

Unique Protocol Identification Number
NCT04058613
Brief Title
Effects of Maintaining Steady Albumin Levels (TAT 4) on Survival and Liver Related Complications in Cirrhosis With Ascites
Official Title
Effects of Maintaining Steady Albumin Levels by Targeted Albumin Therapy (TAT 4) on Survival and Liver Related Complications in Cirrhosis With Ascites and Low Serum Albumin Level- a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2019
Overall Recruitment Status
Unknown status
Study Start Date
September 10, 2019 (Anticipated)
Primary Completion Date
August 8, 2020 (Anticipated)
Study Completion Date
August 8, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Institute of Liver and Biliary Sciences, India

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Investigators intend to assess the utility of regular albumin infusions to maintain a targeted serum albumin level of 4.0 g/dl in newly detected cirrhotic patients with low albumin levels (<2.8g/dl) with ascites.
Detailed Description
Cirrhosis is characterized by progressive deterioration in liver functions. Liver's synthetic functions are inferred by serum albumin and INR estimation. Lower albumin level is a marker of severe liver disease and probability of worsening ascites, hepatorenal syndrome with increased risk for infections. Of the three recent RCTs on utility of long-term administration of albumin, two showed improvement in survival. The studies had included different patient populations (diuretic refractory ascites, high dose diuretics and patients on liver transplant waiting list) with different albumin infusion protocols and different end-points. These studies were done in advanced cases of cirrhosis. There is limited data on the utility of regular albumin infusions in early hepatic decompensation (albumin levels-<2.8g/dl with ascites) and the effect of maintaining a targeted albumin level on survival or liver related side effects. Investigators are trying to address this issue by starting regular albumin infusions at an earlier stage of liver decompensation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Liver Cirrhosis

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
304 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Albumin
Arm Type
Experimental
Arm Description
Albumin infusions will be given at a dose of 40 g twice weekly till a steady albumin level of 4.0g/dl is reached followed by 100ml of 20% albumin at least once in two weeks to maintain a steady albumin level of 4.0g/dl along with the standard medical therapy
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo
Intervention Type
Drug
Intervention Name(s)
ALB Protein, Human
Intervention Description
Albumin infusions will be given at a dose of 40 g twice weekly till a steady albumin level of 4.0g/dl is reached followed by 100ml of 20% albumin at least once in two weeks to maintain a steady albumin level of 4.0g/dl along with the standard medical therapy
Intervention Type
Other
Intervention Name(s)
placebo
Intervention Description
placebo
Primary Outcome Measure Information:
Title
Transplant/Transintrahepatic Portosystemic Shunt (TIPS) free survival in both groups
Description
1 year survival
Time Frame
12 months
Secondary Outcome Measure Information:
Title
New onset refractory ascites in both the groups
Description
refractory ascites is defined as non response to maximum tolerated dose of diuretics
Time Frame
12 months
Title
Spontaneous bacterial peritonitis [SBP] in both groups
Description
Spontaneous bacterial peritonitis is defined as ascitic fluid absolute neutrophil count > 250/ mL with or without culture positivity
Time Frame
12 months
Title
Renal impairment in both groups
Description
serum creatinine concentration >1•5 mg/dL
Time Frame
12 months
Title
Hepatorenal Syndrome in both groups
Description
Hepatorenal Syndrome type 1 is defined as new onset increase in serum creatinine level by 0.3 mg/dL or 50% increase from baseline
Time Frame
12 months
Title
Hepatic encephalopathy grade 3 or 4 in both groups
Description
HE as per West Haven criteria
Time Frame
12 months
Title
Number of new cases with gastrointestinal bleeding in both groups
Description
gastrointestinal bleeding as confirmed by endoscopic/clinical evidence of variceal bleed.
Time Frame
12 months
Title
Requirement of paracentesis in both groups
Description
Ascitic tapping for relieve of pressure symptoms or diagnosis of SBP
Time Frame
12 months
Title
Requirement of diuretics in both groups
Description
Frusemide or Aldactone for management of ascites
Time Frame
12 months
Title
Number of hospitalizations per subject in both groups
Description
Need for any cause hospitalization
Time Frame
12 months
Title
New onset breathlessness/ Hypertension within 24 hours of albumin infusion in both groups
Description
Development of cardiac overload
Time Frame
within 24 hours
Title
Quality of life by Ascite-Q questionnaire in both groups
Description
semiquantitative questionnaire to be answered by the participants
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Newly detected cirrhotic patients aged more than 18 years Cirrhosis defined by standard clinical, analytical and/or histological criteria Serum albumin level < 2.8g/dl with or without ascites Who would agree to give written informed consent Exclusion Criteria: Uncontrolled HTN (sys>150/ dis >90 mmHg) or h/o any drug therapy for HTN Prior h/o Transjugular Intrahepatic Portosystemic Shunt (TIPS) Hepatocellular Carcinoma Active alcohol abuse within 3 months Patients presenting as Acute on Chronic Liver Failure Extrahepatic organ failure Known case of chronic heart failure or respiratory failure Diagnosed Chronic Kidney Disease Patients with hydrothorax Prior liver transplant recipient Human Immunodeficiency Virus infection Use of albumin infusion in the last one month CTP>12, MELD>28 Total Bilirubin >3 g/dl Overt Hepatic Encephalopathy at Presentation
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dr Shasthry SM, MD
Phone
01146300000
Email
shasthry@gmail.com
Facility Information:
Facility Name
Institute of Liver & Biliary Sciences
City
New Delhi
State/Province
Delhi
ZIP/Postal Code
110070
Country
India
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dr Shasthry SM, MD
Phone
01146300000
Email
shasthry@gmail.com

12. IPD Sharing Statement

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Effects of Maintaining Steady Albumin Levels (TAT 4) on Survival and Liver Related Complications in Cirrhosis With Ascites

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