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Superb Microvascular Imaging in Focal Nodular Hyperplasia

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Samsung Medical Center

Status

Completed

Conditions

Focal Nodular Hyperplasia

Treatments

Device: Superb-Microvascular imaging
Drug: Sonazoid

Study type

Interventional

Funder types

Other

Identifiers

NCT02737865
2015-10-134-003

Details and patient eligibility

About

Focal nodular hyperplasia (FNH) in liver is the second common benign hepatic tumor. It usually shows hypervascular mass on imaging studies and it is not easy to differentiate with other hypervascular malignant tumor. For diagnosis of FNH, contrast-enhanced ultrasonography (US) has been used to detect 'spoke-wheel sign', which can be typically seen in FNH. However, temporal window of vascular phase using contrast-enhanced US (CEUS) is very short (about 10 sec) and coordination of patient's respiration during US exam is absolutely needed. Thus, the investigators will use Superb-Microvascular imaging (SMI, Toshiba, Japan) for detection of 'spoke-wheel sign' in patients with proven FNH, which enable to detect slow micro vascular flow without using CEUS.

First, to compare the detection rate of 'spoke-wheel sign' between CEUS using sonazoid (Perfluorobutane, GE healthcare) and SMI.

Second, to compare the accuracy of size measurement between gray-scale US and SMI (reference standard: CEUS using sonazoid.)

Full description

  1. To evaluate the detection rate of 'spoke-wheel sign' on CEUS using sonazoid and SMI (primary outcome).

    Each US findings during exam for patients with FNH were recorded by radiologist. The results were interpreted by consensus using 4 scale bar.

    1. Absence of 'spoke-wheel sign'
    2. Mild suspicious of 'spoke-wheel sign'
    3. Highly suspicious of 'spoke-wheel sign'
    4. Definite "spoke-wheel sign'
  2. To evaluated the accuracy of size measurement for FNH on gray-scale US and SMI (reference standard: CEUS using sonazoid).

    To calculate the measurement error between each method and CEUS using sonazoid on US images using measurement of maximum diameter of tumor.

  3. Sample size calculation according to the primary outcome.

Expecting the detection rate of "spoke-wheel sign" on SMI, 20% (known detection rate on CEUS using sonazoid, 23.5%), a sample size of 62 patients was required using 95% confidence interval.

Enrollment

62 patients

Sex

All

Ages

20 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients with biopsy or imaging proven focal nodular hyperplasia

Exclusion criteria

  1. Pregnant women
  2. Patient's age > 70
  3. Egg allergy
  4. Breast-feeding women

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

62 participants in 1 patient group

SMI and sonazoid (single arm)
Experimental group
Description:
Patients with focal nodular hyperplasia will undergo ultrasonography with Superb-Microvascular imaging and additional sonazoid-enhanced ultrasonography. SMI is a software function in a Toshiba Aplio 500 system. Sonazoid is contrast-material for US and it is a intervention for patient with FNH. Sonazoid will be administered at a dose of 0.015 mL/kg by manual bolus injection, followed by a 10 mL normal saline flush via a peripheral venous line
Treatment:
Drug: Sonazoid
Device: Superb-Microvascular imaging

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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