Actively Recruiting
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
Eligibility Criteria
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.
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
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Complete this quick 3-step screening to check your eligibility
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
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
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