About this trial
Liver disease, a major global health burden, ranges from mild dysfunction to severe conditions like cirrhosis and hepatocellular carcinoma (HCC), the fifth most common cancer. Accurate diagnosis of liver lesions-distinguishing benign from malignant-is vital for treatment planning. Conventional imaging (ultrasound, CT, MRI) has limitations in sensitivity and detecting small metastases. PET/CT combines metabolic and anatomical data but struggles with small lesions and cirrhotic livers.
18F-FDG PET/MRI with contrast-enhanced MRI may improve diagnostic accuracy, but its clinical benefits remain uncertain. Further research is needed to evaluate its performance, impact on patient outcomes, and cost-effectiveness in liver disease management.
Eligibility criteria
Qualifiers
Age ≥18 years;
Patients with suspected liver metastases or hepatic lesions,
Ability to undergo 18F-FDG PET/MRI examination;
Willingness to comply with study protocols.
Disqualifiers
Patients with a history of allergic reactions to MRI contrast agents;
Pregnant or lactating women;
Patients with severe comorbidities, including: Cardiac disease,Renal failure,or Hepatic failure (Child-Pugh C);
Patients unable to cooperate with PET/MRI procedures.
Trial design
Treatments tested in this trial
- Not listed