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Contrast-Enhanced ultrasound (CEUS) for diagnosis of hepatocellular carcinoma (HCC) in at risk patients: a within-patient comparison of SonoVue versus Sonazoid

Contrast-Enhanced ultrasound (CEUS) for diagnosis of hepatocellular carcinoma (HCC) in at risk patients: a within-patient comparison of SonoVue versus Sonazoid

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100052185
Enrollment
Unknown
Registered
2021-10-22
Start date
2021-10-13
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

hepatocellular carcinoma

Interventions

Gold Standard:SonoVue
Index test:Sonazoid

Sponsors

The First Medical Centre, Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Older than 18 years old; 2. Patients have been diagnosed with liver cirrhosis or chronic hepatitis, and is currently undergoing diagnosis/exclusion assessment of HCC; 3. In the 30 days before enrollment in the study, target lesion (at least one FLL >= 1 cm but not greater than 3 cm) was determined in the ultrasound (US) examination, and the lesion needs to be further examined for qualitative diagnosis; 4. Patients Plan to undergo surgery or biopsy of the target lesion, or plan to perform other imaging examinations (CT and/or MRI) to obtain independent reference standards; 5. Obtain informed consent of patients for examination and treatment.

Exclusion criteria

Exclusion criteria: 1. Patients with liver cirrhosis caused by congenital liver fibrosis or vascular disease; 2. The target lesion has been treated (local treatment); 3. According to the product specification, the patient has contraindications to one or two study drug injections; 4. Participated in this study; 5. Pregnant or lactating women; 6. There are any medical conditions or other conditions that will significantly reduce the availability of reliable data, achieve research goals, or complete the research and/or follow-up evaluation.

Design outcomes

Primary

MeasureTime frame
Characteristics of routine ultrasound in liver lesion;Characteristics of contrast-enhanced ultrasound in liver lesion;

Countries

China

Contacts

Public ContactFei Xiang

The First Medical Centre, Chinese PLA General Hospital

george301feixiang@163.com+86 10 66936848

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026