🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in China / NCT06816212
Enrolling by invitation Observational

Correlation Between CEUS Identification of Nodular HPD on CE-MRI and Hepatic Malignant Lesions

NCT06816212 · tracked via the Priya Life Science China tracker
Sponsor
Second Affiliated Hospital, Zhejiang University, School of Medicine
Phase
Observational
Started
2025-02-10
Last updated
2025-02-10

Condition(s) studied

Hepatic Malignant TumorsHepatic Perfusion Disorders

Study summary

Hepatic malignant tumors are a category of diseases with high incidence and mortality rates worldwide, including various types such as primary hepatocellular carcinoma (HCC), intrahepatic cholangiocarcinoma (ICC), and liver metastases. With the advancement of imaging technology, the number of hepatic perfusion disorders (HPD) detected in high-risk population screening and follow-up has gradually increased. However, the imaging manifestations of these HPD are highly heterogeneous, and the imaging features of some benign lesions (such as post-treatment inflammatory reactions, arterioportal shunts, hyperplastic nodules, focal fat deposition or fibrotic nodules) overlap with those of malignant lesions, posing a challenge to accurate diagnosis. Therefore, how to improve the ability to distinguish the benign and malignant nature of HPD based on multimodal imaging technology and optimize the follow-up management of high-risk populations has significant clinical value.

Eligibility

Sex
ALL
Min age
Max age
Healthy volunteers
No
Inclusion Criteria: * Prospective cohort patients voluntarily sign the informed consent form. * Patients with a history of malignant tumors, CE-MRI indicated the presence of HPD in the liver. * The shape of HPD is nodular. * The diameter of HPD is greater than 10mm. * The main large vessels in the liver are clearly displayed in the MRI. Exclusion Criteria: * Patients who unable to complete imaging examinations, such as severe cardiac insufficiency, severe renal insufficiency, hypersensitivity to contrast agents or adverse reactions to them, etc. * Patients with the history of extensive liver resection or liver transplantation. * Patients whose abdomen with abundant intestinal gas.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Department of Ultrasound, Second Affiliated Hospital, School of Medicine, Zhejiang University Hangzhou Zhejiang

More Second Affiliated Hospital, Zhejiang University, School of Medicine trials in China

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06816212 on ClinicalTrials.gov ↗ ← All trials in China