Multicenter Clinical Study on Noninvasive Assessment of Hepatic Steatosis and Fibrosis Using Visual Transient Elastography

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorXinhua Hospital, Shanghai Jiao Tong University School of Medicine

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 volunteers

Qualifiers

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

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

  • Visual Transient Elastography (ViTE) Examination

    Other intervention

    Post-marketing product (Mindray Hepatus 9 Ultrasound Diagnostic System) for visual transient elastography examination in patients with liver injury.

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

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).

Time frame
baseline

Secondary outcomes

Other outcomes

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