Clinical Trials Directory

Trials / Completed

CompletedNCT00777725

Non-invasive Assessment of Liver Stiffness/Fibrosis by Transient Elastography (Fibroscan) in Patients With Left and/or Right Sided Heart Failure

Status
Completed
Phase
Study type
Observational
Enrollment
125 (actual)
Sponsor
Monash University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

This study will involve 70 patients who attend the Alfred Hospital with acute or chronic heart failure as well as 30 age and gender matched control subjects. All participants will have their history taking and a physical examination to detect symptoms and signs of heart failure. The main objectives are for determining the benefit and usefulness of Fibroscan (Liver scan) in detecting liver stiffness (a condition caused by excess fluid build up in the liver which has a negative impact on the livers ability to function properly) in heart failure patients and for characterizing the incidence and severity of liver stiffness in this group of patients. After informed consent, a blood sample will be taken from all patients to assess their full blood examination, glucose, lipid profiles, renal function and so on. Then 24-48 hours after enrollment, the liver doctors will do the liver scan (Fibroscan) by transient elastography. All the data are recorded and further analysis will be assessed. In a small group of acute patients the blood tests and liver scan will be repeated just prior to their discharge. Optional Sub-study: For participants who consent to the optional sub-study another 20 ml of blood for serum liver fibrotic markers will be collected.

Conditions

Interventions

TypeNameDescription
DEVICEFibroScanLiver scan, similar to an ultrasound.

Timeline

Start date
2009-01-01
Primary completion
2010-10-01
Completion
2011-03-01
First posted
2008-10-22
Last updated
2011-07-21

Locations

1 site across 1 country: Australia

Source: ClinicalTrials.gov record NCT00777725. Inclusion in this directory is not an endorsement.