Actively Recruiting

Phase 4
Age: 0 - 18Years
All Genders
NCT06639828

Phase 4 Paediatric Study to Evaluate Sonazoid Safety and Efficacy for Contrast-Enhanced Ultrasound Liver Imaging

Led by GE Healthcare · Updated on 2026-03-04

50

Participants Needed

6

Research Sites

92 weeks

Total Duration

On this page

Sponsors

G

GE Healthcare

Lead Sponsor

P

PPD Development, LP

Collaborating Sponsor

AI-Summary

What this Trial Is About

Liver tumours, 40% of which are benign, account for 1% to 4% of all solid tumours in children. The benign tumours are mainly haemangiomas, liver hamartomas, and liver cell adenomas. The malignant tumours are mainly hepatoblastoma, hepatocellular carcinoma (HCC), malignant liver mesothelioma, and rhabdomyosarcoma. The differential diagnosis of liver masses in children is generally based on the child's age, the clinical evaluation (including alpha-fetoprotein test results), and imaging characteristics. Liver tumours seldom produce clear symptoms and signs in the early stages, and they progress rapidly. As a result, most liver tumours are not diagnosed until the middle or late stages. To improve survival among patients with liver tumours, clinicians must find the liver tumours as early as possible and determine whether the tumours are benign or malignant. Conventional ultrasonography is commonly used for screening, and is preferred as the first-line imaging technique for children. Not only does it have a wide range of applications and a high diagnostic yield, but it is well accepted by patients and their parents. It can be performed in the examination room with the parents present, allowing real-time imaging and direct interaction with patient and parents. CEUS is a non-invasive imaging technology that can continuously and dynamically observe blood perfusion in tumours in real-time through injection of a contrast agent to enhance the blood flow reflux signal in the human body. Consequently, CEUS is useful for visualising capillaries and tissue perfusion in the human body. The purpose of this current study is to evaluate the use of Sonazoid™ perfluorobutane (PFB) microbubbles as a contrast medium for CEUS for evaluation of solitary liver masses in children.

CONDITIONS

Official Title

Phase 4 Paediatric Study to Evaluate Sonazoid Safety and Efficacy for Contrast-Enhanced Ultrasound Liver Imaging

Who Can Participate

Age: 0 - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • The subject is under 18 years of age on the day of consent.
  • The subject has at least 1 untreated focal liver lesion with 8 or fewer lesions (excluding cysts), each 8 cm or smaller, confirmed within the past month (or past 3 months if benign) and visible on ultrasound.
  • The subject has had or is scheduled for a dynamic CT or MRI scan within one month of study inclusion.
  • The subject can follow study procedures.
  • Parents or legal representatives have signed informed consent; patients able to assent have signed an age-appropriate assent form.
  • Post-menarcheal females have a negative urine pregnancy test at screening and before dosing.
  • Post-menarcheal females and sexually active males with partners of childbearing potential practice abstinence or effective birth control for at least 30 days before enrollment.
  • The subject weighs 3 kg or more.
  • The subject has a negative egg allergy test if egg allergy status is unknown.
Not Eligible

You will not qualify if you...

  • Known or suspected hypersensitivity to Sonazoid components, including egg allergies causing severe reactions.
  • Acute life-threatening condition with expected survival of 6 months or less.
  • Received Sonazoid or another ultrasound contrast agent within the past 30 days.
  • Underwent or plans to undergo contrast agent examinations (CT, MRI, or ultrasound) within 24 hours before or after Sonazoid injection.
  • Currently undergoing or has undergone systemic or local chemotherapy or radiation therapy.
  • Participating in another clinical trial involving unregistered drugs or completed such trial less than 30 days ago.
  • Pregnant or breastfeeding females.
  • Physician judges that insertion of a large enough needle (24-gauge or larger) is not possible.
  • Known right-to-left cardiac shunt.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 6 locations

1

Munich University Hospital

München, Germany, 81377

Not Yet Recruiting

2

Papa Giovanni XXIII Hospital

Bergamo, Italy, 24127

Not Yet Recruiting

3

Giannina Gaslini Institute

Genoa, Italy, 16147

Not Yet Recruiting

4

University Hospitals Bristol and Weston NHS Foundation Trust

Bristol, United Kingdom, BS2 8BJ

Actively Recruiting

5

King's College Hospital NHS Foundation Trust

London, United Kingdom, SE5 9RS

Actively Recruiting

6

Imperial College Healthcare NHS Trust

London, United Kingdom, W2 1NY

Actively Recruiting

Loading map...

Research Team

T

Tingting Wang

CONTACT

D

David Thompson

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here