Contrast-enhanced Ultrasound Evaluation of Chemoembolization
NCT02764801 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 131
Last updated 2025-05-06
Summary
The primary objective of this trial is to evaluate the sensitivity and specificity of 2D and 4D contrast enhanced ultrasound for monitoring transarterial chemoembolization (TACE) response 1-2 weeks and 1 month post treatment as an alternative to contrast-enhanced magnetic resonance (MRI) or computed tomography (CT) imaging
Conditions
- Hepatocellular Carcinoma
- Chemoembolization, Therapeutic
Interventions
- DRUG
-
Ultrasound contrast agent (Contrast-enhanced ultrasound)
Intravenous injection of ultrasound contrast agent followed by saline flush though an angiocatheter in the arm or hand.
- DEVICE
-
Logiq E9 Scanner (Contrast-enhanced ultrasound)
Ultrasound scanning using a commercial scanner with a C1-5-D broad-spectrum convex transducer followed by a RAB2-5-D broad-spectrum real-time 4D transducer.
Sponsors & Collaborators
-
University of California, San Diego
collaborator OTHER -
Vanderbilt University Medical Center
collaborator OTHER -
National Institutes of Health (NIH)
collaborator NIH -
Lantheus Medical Imaging
collaborator INDUSTRY -
GE Healthcare
collaborator INDUSTRY -
National Cancer Institute (NCI)
collaborator NIH -
Sidney Kimmel Cancer Center at Thomas Jefferson University
lead OTHER
Principal Investigators
-
John Eisenbrey, PhD · Thomas Jefferson University
Study Design
- Allocation
- NA
- Purpose
- DIAGNOSTIC
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 21 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2016-04-30
- Primary Completion
- 2021-12-31
- Completion
- 2023-02-01
Countries
- United States
Study Locations
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