CEUS Evaluation of Hypoxic Ischemic Injury

PHASE3CompletedINTERVENTIONAL
Enrollment

1

Participants

Timeline

Start Date

December 1, 2020

Primary Completion Date

May 7, 2024

Study Completion Date

May 7, 2024

Conditions
Hypoxic-Ischemic EncephalopathyBrain Ischemia Hypoxia
Interventions
DRUG

Sulfur hexafluoride lipid-type A microspheres

Injection of Sulfur hexafluoride lipid-type A microspheres (Lumason) contrast agent will be performed via the existing peripheral intravenous line using the FDA-recommended dose of 0.03 mg/kg.

Trial Locations (1)

19104

The Children's Hospital of Philadelphia, Philadelphia

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Bracco Diagnostics, Inc

INDUSTRY

lead

Children's Hospital of Philadelphia

OTHER