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Diagnostic Efficacies of Sonazoid-CEUS and EOB-MRI in Patients With High Risk of HCC

A Single-center, Prospective Controlled Study of the Diagnostic Efficacies of Sonazoid-CEUS and EOB-MRI in Patients With High Risk of HCC

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04212273
Enrollment
200
Registered
2019-12-26
Start date
2019-12-21
Completion date
2022-12-24
Last updated
2022-12-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diagnoses Disease, Hepatocellular Cancer, Liver Cirrhoses

Keywords

Hepatocellular carcinoma, Sonazoid Contrast-enhanced ultrasound, EOB-MRI, Diagnostic Efficacy

Brief summary

Hepatocellular carcinoma (HCC) is the fifth most common cancer. Patients with HCCs usually have a poor prognosis. Hepatocarcinogenesis is an intricate and multistep process. Detecting and staging early HCC in patients with liver cirrhosis are still challenging for imaging techniques. Contrast-enhanced ultrasonography (CEUS) and gadoxetic acid-enhanced magnetic resonance imaging (EOB-MRI) are widely used in clinical practice. EOB-MRI has advantages of high detecting rate for small lesions, high sensitivity of hepatobiliary phase and extensive image information. Sonazoid has the advantage of offering a unique post-vascular phase, also called the Kupffer phase. Therefore, malignant tumors with few or no Kupffer cells appear as contrast defects, with respect to the relatively well-enhanced surrounding liver in the postvascular phase. The diagnostic efficacies of these two imaging methods have not been well studied. Therefore, the purpose of this study is to compare the efficacies of Sonazoid-CEUS and EOB-MRI in patients with high risk of HCC, and to compare the detection ability for malignant tumors by Kupffer phase and hepatobiliary phase.

Interventions

DIAGNOSTIC_TESTDiagnostic Sonazoid-CEUS and EOB-MRI

Undergo Sonazoid-CEUS and EOB-MRI

Sponsors

Tianjin Third Central Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Patients are at high risk for HCC. 2. The ages of patients are between 18 and 80. 3. Patients are with solid liver lesion(s) detected by US: if a patient has a solitary tumor, the size of the tumor is less than or equal to 5 cm; if a patient has multiple lesions, the sizes of the tumors are less than or equal to 3 cm and the number of lesions is less than or equal to 3. 4. Patient is able and willing to receive CEUS and EOB-MRI examinations within 30 days. 5. Patient signs the informed consent. -

Exclusion criteria

1. Patient is with lesions confirmed by pathology or follow-up, or hemangiomas. 2. Patient is with lesions already undergoing local treatment, including thermal ablation or TACE. 3. Patient is with severe cardiopulmonary insufficiency. 4. Patient is a pregnant or breastfeeding women. 5. Patient is considered to be unsuitable to participate in the study.

Design outcomes

Primary

MeasureTime frameDescription
The sensitivity, specificity and accuracy of Sonazoid-CEUS and EOB-MRI6 to 12 monthsThe sensitivity, specificity and accuracy of Sonazoid-CEUS and EOB-MRI in the diagnosis for patients with high risk of HCC will be determined.

Secondary

MeasureTime frameDescription
The detection rate of the additionally found HCC6 to 12 monthsThe detection rate of the additionally found HCC on Sonazoid-CEUS and EOB-MRI will be determined .

Countries

China

Contacts

Primary ContactXiang Jing, MD
dr.jingxiang@aliyun.com02284112323
Backup ContactYan Zhou
zhouyan2626@163.com02284118101

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026