Cirrhosis Clinical Trial
Official title:
Prediction of Hepatic Fibrosis in Patients With Chronic Hepatitis C by Biochemical and Duplex Doppler Indices
The purpose of our prospective study was to evaluate the value of Doppler parameters and compare the diagnostic accuracy of Doppler parameters with various biochemical indices in predicting significant hepatic fibrosis (≥ F2) and cirrhosis (F4) in chronic hepatitis C (CHC) patients.
Chronic hepatitis C virus (HCV) infection is a global health problem, affecting about 3% of
the world's population. Compared to patients with mild hepatic fibrosis, those with
significant fibrosis are at risk of developing cirrhosis over a 10- to 20-year period. This
fact suggests the need of early antiviral therapy in chronic hepatitis C (CHC) patients to
prevent the development of cirrhosis and associated complications. For patients having
cirrhosis, surveillance endoscopy and ultrasound for gastroesophageal varices and
hepatocellular carcinoma are needed to minimize morbidity and mortality ). Furthermore,
reduced treatment response and tolerability to antiviral therapy may be encountered in
cirrhotic patients. An accurate assessment of hepatic fibrosis stage is therefore important
for both diagnostic and therapeutic purposes.
Liver biopsy has been recognized as the gold standard for assessing the grade of
necroinflammation and stage of fibrosis. However, it is costly, and harbors risk of
complications, including 20% of patient discomfort, 0.1-3% of significant morbidity, and
0.02-0.24% of mortality. In addition, sampling error due to the non-uniform distribution of
the parenchymal damage, as well as intra- and inter-observer variability is often
encountered. A noninvasive tool to evaluate liver disease activity or fibrosis stage would
be helpful, particularly in monitoring CHC patients over time.
Noninvasive methods to evaluate the hepatic histology in HCV-infected patients include
symptoms and signs, routine laboratory tests, serum markers of fibrosis and inflammation,
quantitative tests of liver function, and radiological imaging. Previous studies have
assessed the usefulness of noninvasive tests in predicting hepatic fibrosis. However, none
of them showed satisfactory results, either due to lack of accuracy, accessibility,
reproducibility or being expensive.
Duplex Doppler ultrasonography (DDU), which is readily available and non-invasive, has been
used for the assessment of splanchnic vascular hemodynamics in patients with chronic liver
disease. Portal vein velocity (PVV) has been shown to be correlated with significant
fibrosis or cirrhosis. Hepatic artery resistive index (HARI) and pulsatility index (HAPI)
are associated with portal vein resistance and hepatic vein-portal vein pressure gradient
(HPVG). Splenic artery resistive index (SARI) and pulsatility index (SAPI) are associated
with portal vein resistance, cirrhosis and grade of esophageal varices (EV). Previous
studies to evaluate the value of DDU in predicting liver histology are controversial,
probably due to small patient number, diverse grading of liver histology, and large missing
data.
Thus, the purpose of our prospective study was to evaluate the value of Doppler parameters
and compare the diagnostic accuracy of Doppler parameters with various biochemical indices
in predicting significant hepatic fibrosis (≥ F2) and cirrhosis (F4) in chronic hepatitis C
(CHC) patients.
;
Observational Model: Case-Only, Time Perspective: Cross-Sectional
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT01884415 -
Phase III, Study to Evaluate the Efficacy of Two Different HBV Vaccination Schemes in Patients With Hepatic Cirrhosis
|
Phase 3 | |
Recruiting |
NCT05014594 -
Sodium-glucose Linked Transporter 2 (SGLT-2) Inhibitors in Recurrent Ascites: a Pilot RCT
|
Phase 2 | |
Not yet recruiting |
NCT03631147 -
The Effect of Rifaximin on Portal Vein Thrombosis
|
N/A | |
Completed |
NCT04939350 -
Evaluation of the Vaccination Coverage of Cirrhotic Patients Followed in the General Hospitals in France in 2021
|
||
Completed |
NCT02528760 -
To Determine the Role of Prokinetics in Feed Intolerance in Critically Ill Cirrhosis
|
N/A | |
Recruiting |
NCT05484206 -
Effect of Hepatic Impairment on the Pharmacokinetics and Safety of VIR-2218 and VIR-3434
|
Phase 1 | |
Not yet recruiting |
NCT05538546 -
Baveno VI Criteria in Dynamic Monitoring of High-risk Varices in Compensated Cirrhotic Patients
|
||
Not yet recruiting |
NCT04053231 -
Hepatocarcinoma Recurrence on the Liver Study - Part2
|
||
Recruiting |
NCT02983968 -
Use of the French Healthcare Insurance Database
|
||
Completed |
NCT02705534 -
Sofosbuvir, Ledipasvir, Ribavirin for Hepatitis C Cirrhotics, Genotype 1
|
Phase 3 | |
Completed |
NCT02596880 -
Sofosbuvir, Daclatasvir, Ribavirin for Hepatitis C Virus (HCV) Cirrhotics
|
Phase 3 | |
Completed |
NCT02247414 -
Warfarin Prevents Portal Vein Thrombosis in Patients After Laparoscopic Splenectomy and Azygoportal Disconnection
|
Phase 4 | |
Completed |
NCT02016196 -
Rifaximin vs Placebo for the Prevention of Encephalopathy in Patients Treated by TIPS
|
Phase 3 | |
Withdrawn |
NCT01956864 -
Study of High-Dose Oral Vitamin D for the Prevention of Liver Cancer
|
Phase 1 | |
Completed |
NCT02113631 -
Comparative Effectiveness and Tolerability of Boceprevir vs Telaprevir
|
N/A | |
Completed |
NCT01362855 -
Advance Care Planning Evaluation in Hospitalized Elderly Patients
|
||
Completed |
NCT01447537 -
Mechanisms Involved in the Benefits of an Exercise Programme in Patients With Cirrhosis
|
N/A | |
Active, not recruiting |
NCT01205074 -
¹³C-Methacetin Breath Test (MBT) Methodology Study
|
Phase 2/Phase 3 | |
Completed |
NCT01476995 -
Prognostic Indicators as Provided by the EPIC ClearView
|
N/A | |
Completed |
NCT01231828 -
Method of Assessment of Driving Ability in Patients Suffering From Wakefulness Pathologies.
|
N/A |