search
Back to results

Brain Imaging in Patients With Chronic Liver Disease and Functional Impairment.

Primary Purpose

Cirrhosis, Hepatic Encephalopathy

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
l-ornithine l-aspartate
Sponsored by
Imperial College London
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Cirrhosis focused on measuring magnetic resonance imaging, magnetic resonance spectroscopy, functional magnetic resonance imaging, cirrhosis, hepatic encephalopathy, l-ornithine l-aspartate

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Age 18-65 Biopsy-proven cirrhosis Clinically stable Able to give informed consent Fluent English (required for psychometric testing) Exclusion Criteria: Ferro-magnetic implants Claustrophobia Weight >120kg Significant renal impairment (Creatinine >150 micromol/L) Poorly controlled Diabetes (particularly type I with microvascular complications) Alcohol: if alcoholic liver disease is the aetiology of their liver disease they should be abstinent. Otherwise less than 20g per day.

Sites / Locations

  • Imperial College London

Outcomes

Primary Outcome Measures

All enrolled patients will be given 4 weeks of treatment. Both MRI and functional changes will be observed.

Secondary Outcome Measures

Full Information

First Posted
March 21, 2006
Last Updated
May 28, 2015
Sponsor
Imperial College London
Collaborators
Royal College of Physicians, Paddington Charitable Estates Educational Fund, University of London
search

1. Study Identification

Unique Protocol Identification Number
NCT00305591
Brief Title
Brain Imaging in Patients With Chronic Liver Disease and Functional Impairment.
Official Title
Functional Magnetic Resonance Imaging and Spectroscopy of the Brain in Patients With Chronic Hepatic Encephalopathy
Study Type
Interventional

2. Study Status

Record Verification Date
January 2008
Overall Recruitment Status
Completed
Study Start Date
March 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
October 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Imperial College London
Collaborators
Royal College of Physicians, Paddington Charitable Estates Educational Fund, University of London

4. Oversight

5. Study Description

Brief Summary
Hepatic encephalopathy (HE) is a frequent complication of chronic liver disease (cirrhosis) and involves a wide spectrum of problems from mild impairment of reaction times in driving and operating machinery through to disturbances in mood, behaviour and conscious levels. Magnetic resonance imaging (MRI) is a method of obtaining pictures of the inside of the body. Patients with liver disease have previously been studied with MRI which has highlighted changes in the brain. This research aims to highlight some of the differences in the way that the brain functions in patients with liver disease. Using our new, more powerful MRI scanner, with more sophisticated techniques we hope that the novel combination of MRI techniques can objectively detect the presence of , and monitor HE. Study hypothesis: Hepatic encephalopathy (HE) is a reversible, metabolic disturbance of the brain, associated with low grade brain swelling and disturbances of the chemical balance within the brain, resulting in functional impairment, the presence of which MR imaging can detect with sufficient sensitivity to monitor the changes that may occur over time in response to treatment.
Detailed Description
Hepatic encephalopathy (HE) is a common neuropsychiatric abnormality, complicating the course of liver disease patients. In the UK, cirrhosis accounts for 4000 deaths per year, and 500,000 people are thought to be infected with chronic hepatitis C, of which up to 20% will develop cirrhosis over 20 years. The condition has been difficult to monitor objectively. Despite the fact that the syndrome was probably first recognised two thousand years ago, the exact pathogenesis still remains unclear. It is thought to represent a reversible disturbance in brain chemistry and consequent brain swelling, in response to blood containing unfiltered gut-derived toxins entering the cerebral circulation. There is no recognised 'gold standard' test to diagnose and monitor this important, disabling condition. I have developed a novel combination of magnetic resonance imaging (MRI) sequences at 3 Tesla to study the effects of hepatic encephalopathy on the brain in patients with cirrhosis. We propose to investigate alterations in brain size, function and chemistry before, and then at intervals after 4 weeks anti-encephalopathy treatment with L-ornithine L-aspartate. This will enable the assessment of both the baseline brain alterations of the cohort and the brain's response to therapy and correlation with their clinical response. As such this longitudinal study would allow us to define the sensitivity of the MR techniques. Each of 50 patients will have blood tests, a 1 hour MRI brain scan and psychometric testing. The psychometric testing will be performed with both a computer-based battery and conventional paer-based tests. They will then be given L-ornithine L-aspartate (LOLA) to take orally for 4 weeks and have repeat blood tests, MRI and psychometric tests. We will then determine if there is a correlation between the MR data and the results of the psychometric testing.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cirrhosis, Hepatic Encephalopathy
Keywords
magnetic resonance imaging, magnetic resonance spectroscopy, functional magnetic resonance imaging, cirrhosis, hepatic encephalopathy, l-ornithine l-aspartate

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
l-ornithine l-aspartate
Primary Outcome Measure Information:
Title
All enrolled patients will be given 4 weeks of treatment. Both MRI and functional changes will be observed.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age 18-65 Biopsy-proven cirrhosis Clinically stable Able to give informed consent Fluent English (required for psychometric testing) Exclusion Criteria: Ferro-magnetic implants Claustrophobia Weight >120kg Significant renal impairment (Creatinine >150 micromol/L) Poorly controlled Diabetes (particularly type I with microvascular complications) Alcohol: if alcoholic liver disease is the aetiology of their liver disease they should be abstinent. Otherwise less than 20g per day.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Simon D Taylor-Robinson, MBBS, FRCP
Organizational Affiliation
Imperial College London & St Mary's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Imperial College London
City
Hammersmith
State/Province
London
ZIP/Postal Code
W12 0HS
Country
United Kingdom

12. IPD Sharing Statement

Learn more about this trial

Brain Imaging in Patients With Chronic Liver Disease and Functional Impairment.

We'll reach out to this number within 24 hrs