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Contrast-enhanced Ultrasound With Perfluorobutane and Sulfur Hexafluoride for Hepatocellular Carcinoma

Seoul National University logo

Seoul National University

Status

Completed

Conditions

Hepatocellular Carcinoma

Treatments

Diagnostic Test: contrast enhanced ultrasound
Diagnostic Test: Liver MRI
Diagnostic Test: Dynamic CT

Study type

Interventional

Funder types

Other

Identifiers

NCT04847726
SNUH-1807-166

Details and patient eligibility

About

Intra-individual comparison of diagnostic performance of CEUS With perfluorobutane and sulfur hexafluoride for HCC in high-risk Individuals, and their role in the diagnostic algorithm of HCC.

Full description

The investigators would compare the diagnostic performance for HCC at high-risk individuals between both USG contrast agents.

Enrollment

110 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • high-risk for HCC (liver cirrhosis, chronic hepatitis B)
  • treatment-naive hepatic nodule (>= 1cm) on preceding CT, MR or ultrasound

Exclusion criteria

  • severe cardiopulmonary dysfunction
  • pregnancy
  • refusal to enroll study

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

110 participants in 1 patient group

CEUS with perfluorobutane and sulfur hexafluoride
Experimental group
Description:
Contrast-enhanced ultrasound with perfluorobutane and sulfur hexafluoride for the hepatic lesion.
Treatment:
Diagnostic Test: Liver MRI
Diagnostic Test: contrast enhanced ultrasound
Diagnostic Test: Dynamic CT

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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