Pediatric Intravenous Contrast-Enhanced Ultrasound(CEUS) in China

NCT07113808 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 108

Last updated 2025-12-08

No results posted yet for this study

Summary

The goal of this clinical trial is to evaluate the application of intravenous contrast-enhanced ultrasound examination in children with intra-abdominal diseases that require clear diagnoses. The main questions it aims to answer are:

* Is intravenous contrast-enhanced ultrasound helpful for the diagnosis of intra-abdominal diseases in children?
* What medical problems do participants have when participating in intravenous contrast-enhanced ultrasound examination?
* How can ultrasound doctors conduct intravenous contrast-enhanced ultrasound examinations in a standardized manner? Researchers will performing intravenous contrast-enhanced ultrasound examinations on participants and collecting research subjects to establish a multicenter clinical data database.

Participants will:

* Perform abdominal ultrasound examination to assess the condition.
* At least conduct one intravenous contrast-enhanced ultrasound examination. Based on the result of the contrast examination, decide whether to conduct another examination.
* Keep a diary of their symptoms and therapeutic process in 30 days.

Conditions

  • Abdominal Neoplasm
  • Abdominal Injury
  • Ascites

Interventions

DEVICE

contrast-enhanced ultrasound examination

to evaluate the the application of contrast-enhanced ultrasound examination in children with intra-abdominal diseases that require clear diagnoses aged from 29 days to 18 years old

DRUG

SonoVue®

perform contrast enhanced ultrasound (CEUS) using Sonovue as the contrast agent

Sponsors & Collaborators

  • Shenzhen Children's Hospital

    collaborator OTHER_GOV
  • Children's Hospital of Chongqing Medical University

    collaborator OTHER
  • Tianjin Children's Hospital

    collaborator OTHER
  • Kunming Children's Hospital

    collaborator OTHER
  • Second Affiliated Hospital, School of Medicine, Zhejiang University

    collaborator OTHER
  • West China Hospital

    collaborator OTHER
  • Yuying Children's Hospital of Wenzhou Medical University

    collaborator OTHER
  • Xian Children's Hospital

    collaborator OTHER_GOV
  • The Children's Hospital of Zhejiang University School of Medicine

    lead OTHER

Eligibility

Min Age
29 Days
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-09-10
Primary Completion
2026-09-30
Completion
2026-09-30
FDA Drug
Yes

Countries

  • China

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07113808 on ClinicalTrials.gov