National Taiwan University Hospital
Taipei, Taiwan
NCT Number: NCT07675187
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.
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Not applicable
Taipei, Taiwan
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
GAAD score (Gender, age, AFP, DC) will be measured every 6 months in the GAAD Surveillance Group.
Time frame: From the date of enrollment up to 3 years.
The maximal tumor diameter of all HCC tumors, measured in centimeters
Time frame: From the date of enrollment up to 3 years.
The stage of HCC, using the BCLC staging and the AJCC TNM staging
Time frame: From the date of enrollment up to 3 years
The number of HCC tumors evaluated by abdominal CT or MRI exams
Time frame: From the date of enrollment up to 3 years
The rate of new HCC developed during the study
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.)
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)
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.
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).
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.
Contact information is provided by the study sponsor or research team.
National Taiwan University Hospital
Other
Hepatocellular Carcinoma Risk Assessment and Surveillance in Patients With Type 2 Diabetes
Acronym: GAAD-DM
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