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NCT Number: NCT07675187

HCC Risk and Monitoring in Patients With Type 2 Diabetes

Liver cancer is a significant malignancy in Taiwan. With the widespread implementation of antiviral therapies, hepatitis B and C-related liver cancer has gradually declined; however, metabolic dysfunction-associated liver cancer continues to increase, particularly among patients with type 2 diabetes mellitus (T2DM) who also present with significant liver fibrosis. Current clinical guidelines lack standardized recommendations for liver cancer screening in this specific population, and data from prospective randomized controlled trials remain scarce.This study is a prospective randomized controlled trial enrolling patients aged 18 years, diagnosed with T2DM, and with a FIB-4 > 2.67. Participants will be randomly assigned to either the surveillance group or the standard-care group. The surveillance group will undergo blood tests every 6 months to monitor liver function, AFP, and PIVKA-II, alongside the calculation of the GAAD score. The standard-care group will receive liver function tests every 6 months according to routine clinical practice. Abdominal ultrasound or computed tomography (CT) scans will be arranged by clinicians when clinically indicated. All participants will undergo abdominal ultrasound at baseline and at the end of the third year, with blood samples and clinical data collected periodically. The primary endpoint of this study is the tumor size at the time of liver cancer diagnosis. Secondary endpoints include liver cancer staging, number of liver cancer tumors, liver cancer incidence, the proportion of patients receiving curative treatment, and the degree of liver fibrosis as reflected by changes in FIB-4. This study expects to clarify the clinical benefits of a GAAD score-based surveillance strategy compared to standard care in T2DM patients with high FIB-4 scores, thereby providing evidence-based support for future liver cancer screening strategies and clinical guidelines.

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Key information

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age 18 years or older.
  • Diagnosed with type 2 diabetes mellitus and clinically followed with regular outpatient visits.
  • FIB-4 index greater than 2.67 (calculated based on AST, ALT, and platelet count within the past 6 months).
  • Willing and able to provide written informed consent.

Exclusion criteria

  • HBsAg positive.
  • Anti-HCV positive and HCV RNA positive (patients with anti-HCV positive but negative HCV RNA are still eligible).
  • Prior history of hepatobiliary malignancies.
  • Undergoing regular abdominal ultrasound screening more than once per year.
  • Established diagnosis of liver cirrhosis via abdominal ultrasound or clinical evaluation.
  • Diagnosed with or treated for any malignancy within the past 2 years.
  • Women of childbearing potential or pregnant women.
  • Thrombocytopenia secondary to hematologic disorders.
  • Known history of human immunodeficiency virus (HIV) infection.
  • Concomitant use of medications that may interfere with PIVKA-II assay results (e.g., warfarin, vitamin K).

Treatment and study plan

GAAD score

Diagnostic Test

GAAD score (Gender, age, AFP, DC) will be measured every 6 months in the GAAD Surveillance Group.

Primary outcomes

  1. Maximum tumor diameter of hepatocellular carcinoma (cm).

    Time frame: From the date of enrollment up to 3 years.

    The maximal tumor diameter of all HCC tumors, measured in centimeters

Secondary outcomes

  1. Stage of hepatocellular carcinoma.

    Time frame: From the date of enrollment up to 3 years.

    The stage of HCC, using the BCLC staging and the AJCC TNM staging

  2. Number of hepatocellular carcinoma tumors

    Time frame: From the date of enrollment up to 3 years

    The number of HCC tumors evaluated by abdominal CT or MRI exams

  3. Incidence of hepatocellular carcinoma

    Time frame: From the date of enrollment up to 3 years

    The rate of new HCC developed during the study

  4. Proportion of hepatocellular carcinoma cases receiving curative treatment.

    Time frame: From the date of enrollment up to 3 years.

    Proportion of hepatocellular carcinoma cases receiving curative treatment (including liver transplantation, surgical resection, local ablation, proton therapy, and etc.)

  5. Changes in the degree of liver fibrosis as assessed by the FIB-4 index.

    Time frame: From the date of enrollment up to 3 years.

    The serial FIB-4 level changes during the study period (measured every 6 months)

  6. Participant return-visit rate (adherence to trial follow-up).

    Time frame: From the date of enrollment up to 3 years.

    The rate of patients who adhere to trial follow-up. Calculated by number of visits divided by total number of planned visits.

  7. Incidence of liver cirrhosis.

    Time frame: From the date of enrollment up to 3 years.

    The number of participants who developed liver cirrhosis (diagnosed by FibroScan > 15 kPa, or a clinical diagnosis by ultrasound, CR, or MRI).

  8. Number of computed tomography (CT) or magnetic resonance imaging (MRI) examinations performed for the purpose of hepatocellular carcinoma screening.

    Time frame: From the date of enrollment up to 3 years.

    The total number of computed tomography (CT) or magnetic resonance imaging (MRI) examinations performed for the purpose of hepatocellular carcinoma screening during the study period.

Study contacts

Contact information is provided by the study sponsor or research team.

Tung-Hung Su, PhD

CONTACT

[email protected]

+886-2-23123456

Sponsors and collaborators

Lead sponsor

National Taiwan University Hospital

Other

Registry information

Official study title

Hepatocellular Carcinoma Risk Assessment and Surveillance in Patients With Type 2 Diabetes

Acronym: GAAD-DM

Important dates

Study start
2026
Primary completion
2028
Study completion
2030
First posted
Jun 30, 2026
Registry last updated
Jul 7, 2026

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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