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NCT Number: NCT02476695

FibroTouch Non-invasive Evaluation of Liver Fibrosis and Cirrhosis

This prospective and multicenter study is to determine the diagnostic performance (accuracy, specificity and sensitivity) of transient elastography (FibroTouch) for liver fibrosis assessment in chronic hepatitis B (CHB) patients using ROC analysis, and liver biopsy as the reference.

Actual 517 patients will be enrolled to guarantee 500 final statistical cases; and ≥100 cases are required for fibrosis stage S0/1, S2, S3 and S4 (compensatory stage of cirrhosis), respectively. For each stage, the case is assigned as equally as possible.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Beijing Friendship Hospital, Capital Medical University, Beijing, China

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About this study

The liver diseases frequently occur in China. For various reasons, the chronic liver diseases are not controlled in time, and then develop gradually into liver fibrosis and cirrhosis. Without effective treatment, the advanced liver cirrhosis seriously influences the quality of patients' life, and places an intolerable burden on family and society. At present, the scholars generally thought that the liver fibrosis at early stages is reversible. Therefore, if the liver fibrosis in patients with chronic liver diseases can be accurately evaluated at early stages and be treated in time, so we can stop the progress of diseases and reduce the occurrence of liver cirrhosis and liver cancer.

For many years, liver biopsy is still as "golden standard" for diagnosis of liver inflammation and fibrosis. However, with its invasiveness, potential risks and some complications, liver biopsy is limited in clinical application due to the poor acceptability and repeatability. In recent years, the liver fibrosis cannot directly and accurately diagnose via the various diagnostic models using serological biomarkers (e.g. FIBROTEST and APRI) and medical imaging technologies (e.g. ultrasonic B, CT and MRI).

Transient elastography is a new technology in the field of ultrasonic imaging. Liver stiffness measurement (LSM) is based on the relationship between the speed of spread of acoustic wave in tissues and stiffness of the tissues. It utilizes specific probes to send out controlled low-frequency shear waves, the waves signals transmit through liver tissues, a high-frequency signals will track the transmitting process of shear wave in the liver and the value of liver stiffness (kPa) is quickly calculated with reference to a built-in liver histological model, which provides a quantitative standard for diagnosis of liver fibrosis of chronic liver disease. The bigger LSM value means the faster transmission of shear wave, and the harder of determined liver tissue.

As stated in the "12th Five-year Plan for Medical Device Technological Industry" (the Ministry of Science and Technology), China will greatly support the research and development of new medical devices and promote the application of Chinese transient elastography system, FibroTouch, which was R&D by Tsing-Hua University independently with new algorithm. FibroTouch can rapidly determine the LSM in a non-invasive way and provide useful information for liver fibrosis and steatosis staging.

Due to FibroTouch is a new transient elastography system in marketing, there is no too much studies on the correlation between FibroTouch and liver biopsy in diagnosis of liver fibrosis and cirrhosis.

The goal of this prospective and multicenter study is to determine the diagnostic performance (accuracy, specificity and sensitivity) of FibroTouch for liver fibrosis assessment in chronic hepatitis B (CHB) patients using ROC analysis, and liver biopsy as the reference.

Actual 517 patients will be enrolled to guarantee 500 final statistical cases; and ≥100 cases are required for fibrosis stage S0/1, S2, S3 and S4 (compensatory stage of cirrhosis), respectively. For each stage, the case is assigned as equally as possible.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subjects with age 18-65 years, both gender
  • Subjects with history of HBV or HBsAg positive > 6 months up to enrollment
  • Subjects with qualified liver biopsy specimens within three months (before or after) of Fibrotouch examination for pathological staging
  • Subjects without chemical therapy history of powerful medicine to lower enzyme in the two weeks before blood biochemistry tests (e.g. dimethyl diphenyl bicarboxylate and bicyclol)
  • Subjects must agree and sign the informed consent form

Exclusion criteria

  • Subjects who are unable or unwilling to sign informed consent form
  • Subjects who have merger of hepatitis C, alcohol and non-alcoholic fatty liver diseases, autoimmune liver diseases, inherited metabolic liver diseases, biliary systemic diseases or liver and gall parasitic diseases
  • Subjects who have other serious chronic disorders or history of malignancy
  • Subjects with ALT ≥5 ULN in the past 1 month
  • Subjects with WBC<3.5×10^9/L, PLT<60×10^9/L, PTA<60%
  • Subjects with DBIL≥1.5 ULN
  • Subjects with decompensated cirrhosis (especially the people with ascites)
  • Pregnant or lactating women, or women who has a pregnant plan and don't want to birth control in the study period
  • Subjects who have wound on the right upper abdomen recently
  • Subjects who have various space-occupying tumor or cyst in right liver
  • Subjects who have none or limited legal capacity

Treatment and study plan

FibroTouch Examination

Device

Liver stiffness measurements are performed using FibroTouch and the procedure is non-invasive and painless.

FibroScan Examination

Device

Liver stiffness measurements are performed using another transient elastography, FibroScan, and the procedure is non-invasive and painless.

Ultrasonic B Examination

Device

The ultrasonic B examination is made at an empty stomach for ≥8h. The inner diameter of liver, spleen, gallbladder, portal vein and splenoportal vein is measured through the ordinary two-dimensional ultrasonic examination. The echo data of liver surface/edge/parenchyma and gallbladder wall is scored to evaluate the severity of fibrosis.

Primary outcomes

  1. The Clinical Value Evaluation of FibroTouch for Non-invasive Diagnosis of Liver Fibrosis in Patients With Chronic Hepatitis B by Using Liver Pathology as the Gold Standard for Judging CHB Liver Fibrosis Stage

    Time frame: Participants will be offered a FibroTouch examination before or after taking the test of liver biopsy, and the time interval should not exceed 3 months.

    Altogether 412 patients were included to analyze the diagnostic performance of FibroTouch. The area under the receiver operating characteristic curve for the LSM was 0.846 (95% confidence interval CI 0.808-0.880) for fibrosis stage ≥ F1, 0.850 for ≥ F2, 0.908 for ≥ F3 and 0.874 for F4. Optimal LSM cut-off values for diagnosing fibrosis stage ≥ F1, ≥ F2, ≥ F3, and F4 were 5.5 kPa, 7.85 kPa, 10.0 kPa, and 12.7 kPa, respectively.

Sponsors and collaborators

Lead sponsor

Wuxi Hisky Medical Technology Co Ltd

Industry

Collaborators

  • Beijing Friendship Hospital
  • China-Japan Friendship Hospital
  • Hebei Medical University Third Hospital
  • Henan Provincial People's Hospital
  • Hospital of Chinese Medicine of the Xinjiang Uygur Autonomous Region
  • Jiangsu Provincial People's Hospital
  • No.85 Hospital, Changning, Shanghai, China
  • Peking University Clinical Research Institute (PUCRI)
  • Ruijin Hospital
  • The First Affiliated Hospital of the Fourth Military Medical University
  • The First Affiliated Hospital, Third Military University
  • The First Hospital of Jilin University
  • The Military General Hospital of Beijing, PLA
  • Third Affiliated Hospital, Sun Yat-Sen University
  • Tianjin Third Central Hospital
  • West China Hospital

Registry information

Official study title

Research on FibroTouch Noninvasive Evaluation of Liver Fibrosis and Cirrhosis

Important dates

Study start
2014
Primary completion
2018
Study completion
2018
First posted
Jun 19, 2015
Registry last updated
Mar 5, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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