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Efficacy of Albumin for Acute Encephalopathy in Patients With Cirrhosis (ALFAE)

Primary Purpose

Hepatic Encephalopathy

Status
Completed
Phase
Phase 4
Locations
Spain
Study Type
Interventional
Intervention
Albumin
Sodium chloride 0.9%
Sponsored by
Hospital Universitari Vall d'Hebron Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatic Encephalopathy focused on measuring Hepatic encephalopathy, Cirrhosis, Albumin

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Cirrhosis of the liver
  • Hepatic encephalopathy stage>1
  • Completion of a standardized protocol to investigate precipitating factors
  • Informed consent by next of keen

Exclusion Criteria:

  • Pregnancy
  • Terminal liver disease (advanced liver disease and performance status 3-4 prior to the episode of acute encephalopathy)
  • Need of advanced life support (mechanical ventilation, ionotropic support, dialysis)
  • Need of albumin administration (e.g. bacterial spontaneous peritonitis)
  • Contraindication for albumin administration (e.g. cardiac failure)

Sites / Locations

  • Parc Tauli
  • Hospital de Sant Pau
  • Hospital Universitari Vall d'Hebron
  • Hospital Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Albumin

Saline

Arm Description

Outcomes

Primary Outcome Measures

Proportion of patients without hepatic encephalopathy

Secondary Outcome Measures

Severity of encephalopathy assessed by CHESS and West-Haven

Full Information

First Posted
April 22, 2009
Last Updated
December 14, 2012
Sponsor
Hospital Universitari Vall d'Hebron Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT00886925
Brief Title
Efficacy of Albumin for Acute Encephalopathy in Patients With Cirrhosis
Acronym
ALFAE
Official Title
Effects of the Administration of Albumin in Patients With Cirrhosis and Acute Hepatic Encephalopathy.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2012
Overall Recruitment Status
Completed
Study Start Date
March 2009 (undefined)
Primary Completion Date
July 2012 (Actual)
Study Completion Date
July 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital Universitari Vall d'Hebron Research Institute

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether the administration of albumin in addition to the standard care is effective in the treatment of an episode of hepatic encephalopathy in patients with cirrhosis.
Detailed Description
Hepatic encephalopathy is a frequent complication of cirrhosis that is usually associated with poor prognosis. The most common presentation is an acute episode of hepatic encephalopathy precipitated by factors that increase the exposure of the brain to ammonia. Current therapies are based on measures that decrease plasma ammonia and counteract the effect of factors such as infection or electrolyte's disturbances. Brain edema and abnormalities of cerebral blood flow appear to be important. Part of the impairment of astrocyte function could be related to an increase of oxidative stress injury. In patients with cirrhosis and hepatic encephalopathy, the concentration of albumin in plasma is usually low. Administration of human albumin in patients with hepatorenal syndrome and spontaneous bacterial peritonitis has a major impact on the prognosis of these complications. Albumin prevents circulatory dysfunction and renal failure. The mechanisms of action may include the maintenance of oncotic pressure and a scavenger effect of toxic substances present in blood. Albumin has also shown beneficial effects in neurological injury secondary to stroke, probably in relation to this scavenger effect. The administration of intravenous albumin to patients with hepatic encephalopathy may have beneficial effects on the course of encephalopathy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatic Encephalopathy
Keywords
Hepatic encephalopathy, Cirrhosis, Albumin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
56 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Albumin
Arm Type
Active Comparator
Arm Title
Saline
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Albumin
Intervention Description
Albumin 20%. Day 0: 400-600 ml. Day 2: 200-400 ml.
Intervention Type
Drug
Intervention Name(s)
Sodium chloride 0.9%
Intervention Description
Day 0: 400-600 ml. Day 2: 200-400 ml.
Primary Outcome Measure Information:
Title
Proportion of patients without hepatic encephalopathy
Time Frame
Day 3
Secondary Outcome Measure Information:
Title
Severity of encephalopathy assessed by CHESS and West-Haven
Time Frame
Admission to the hospital (up to day 14)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Cirrhosis of the liver Hepatic encephalopathy stage>1 Completion of a standardized protocol to investigate precipitating factors Informed consent by next of keen Exclusion Criteria: Pregnancy Terminal liver disease (advanced liver disease and performance status 3-4 prior to the episode of acute encephalopathy) Need of advanced life support (mechanical ventilation, ionotropic support, dialysis) Need of albumin administration (e.g. bacterial spontaneous peritonitis) Contraindication for albumin administration (e.g. cardiac failure)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Juan Cordoba, MD
Organizational Affiliation
Hospital Vall d'Hebron
Official's Role
Principal Investigator
Facility Information:
Facility Name
Parc Tauli
City
Sabadell
State/Province
Barcelona
Country
Spain
Facility Name
Hospital de Sant Pau
City
Barcelona
ZIP/Postal Code
08025
Country
Spain
Facility Name
Hospital Universitari Vall d'Hebron
City
Barcelona
ZIP/Postal Code
08035
Country
Spain
Facility Name
Hospital Clinic
City
Barcelona
ZIP/Postal Code
08036
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
23872605
Citation
Simon-Talero M, Garcia-Martinez R, Torrens M, Augustin S, Gomez S, Pereira G, Guevara M, Gines P, Soriano G, Roman E, Sanchez-Delgado J, Ferrer R, Nieto JC, Sunye P, Fuentes I, Esteban R, Cordoba J. Effects of intravenous albumin in patients with cirrhosis and episodic hepatic encephalopathy: a randomized double-blind study. J Hepatol. 2013 Dec;59(6):1184-92. doi: 10.1016/j.jhep.2013.07.020. Epub 2013 Jul 19.
Results Reference
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Efficacy of Albumin for Acute Encephalopathy in Patients With Cirrhosis

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