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NCT03199274CompletedPhase 2

Perflutren Protein-Type A Microspheres and Contrast-Enhanced Ultrasound in Improving Response to Radioembolization Therapy in Patients With Liver Cancer

Ultrasound Microbubble Destruction and Perfusion Quantification for Improving Radioembolization Therapy of Hepatocellular Carcinoma

Source: ClinicalTrials.gov · Last updated 2 Jan 2026

Brief summary (registry, in English)

This phase II trial studies how well perflutren protein-type A microspheres and contrast-enhanced ultrasound work in improving response to radioembolization therapy in patients with liver cancer. Ultrasound contrast agents, such as perflutren protein-type A microspheres, use gas microbubbles to improve image quality. Using contrast-enhanced ultrasound imaging will "pop" these microbubbles and cause tumors to become more sensitive to radiation therapies.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
104 (actual)
First submitted
22 Jun 2017
Start date
1 Jul 2017
Primary completion date
27 Feb 2024
Lead sponsor
Thomas Jefferson University
NCT number
NCT03199274

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 104
  • From 1 Jul 2017 to the primary completion date, 27 Feb 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients who are medically unstable, patients who are seriously or terminally ill, and patients whose clinical course is unpredictable; for example:
    • Patients on life support or in a critical care unit
    • Patients with unstable occlusive disease (e.g., crescendo angina)
    • Patients with clinically unstable cardiac arrhythmias, such as recurrent ventricular tachycardia
    • Patients with uncontrolled congestive heart failure (New York heart Association \[NYHA\] class IV)
  • Patients with recent cerebral hemorrhage
  • Patients with known hypersensitivity to perflutren
  • Patients with known cardiac shunts
  • Patients with known congenital heart defects
  • Patients with severe emphysema, pulmonary vasculitis, or a history of pulmonary embolism
  • Patients with respiratory distress syndrome
  • Patients with a history of bleeding disorders

Lab values

  • Patients with known sensitivities to albumin, blood, or blood products
  • Patients with bilirubin levels \> 2 mg/dL

Other

  • Females who are pregnant or nursing

Who the study is looking for

  • Be scheduled for sub-lobar radioembolization therapy of a previously untreated HCC mass \< 6 cm visible on grayscale ultrasound
  • Be medically stable
  • If a female of child-bearing age, have a negative pregnancy test prior to each ultrasound exam
  • Have signed informed consent to participate in the study

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sidney Kimmel Cancer Center at Thomas Jefferson University
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.