About this trial
Using liver biopsy as the gold standard, this study will conduct visual transient elastography (ViTE) examinations using Mindray Hepatus 9 ultrasound diagnostic system in patients with liver injury to evaluate the diagnostic efficacy of Liver Steatosis Analysis (LiSA) and ViTE for grading hepatic steatosis and fibrosis, and establish corresponding diagnostic thresholds.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Be aged 18-65 years.
Documented liver injury of any etiology with a liver biopsy performed within the past 2 weeks.
Willing to undergo Visual Transient Elastography (ViTE) examination using Mindray Hepatus 9 Ultrasound System and capable of providing written informed consent.
Disqualifiers
Acute viral hepatitis.
Right heart failure with either:Serum transaminases >5× upper limit of normal (ULN),Total bilirubin >85.5 μmol/L.
History of hepatocellular carcinoma (HCC).
Pregnancy.
Trial population
Patients with liver injury
Trial design
Case-only
Prospective
Treatments tested in this trial
Visual Transient Elastography (ViTE) Examination
Other interventionPost-marketing product (Mindray Hepatus 9 Ultrasound Diagnostic System) for visual transient elastography examination in patients with liver injury.
Treatment groups
Trial outcomes
Primary outcomes
The diagnostic performance of LiSA and ViTE was evaluated using the area under the receiver operating characteristic curve (AUROC).
Optimal cutoff values for LiSA and ViTE were determined by maximizing the Youden index, sensitivity (Se), and specificity (Sp). For each cutoff value, the following metrics with 95% confidence intervals (CI) were calculated: sensitivity (Se), specificity (Sp), positive predictive value (PPV), and negative predictive value (NPV).
Sponsors and contacts
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Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Lead sponsor
Shenzhen Mindray Bio-Medical Electronics Co., Ltd
Collaborator