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Study identifier: NCT06693752 Synced from ClinicalTrials.gov · July 29, 2026
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CEUS Evaluation of Hydrocephalus in Neonates and Infants

Condition: Hydrocephalus in Infants · Hydrocephalus Acquired  ·  Sponsor: Children's Hospital of Philadelphia

PhasePhase 2
Planned participants20
Who can joinAll sexes, 1 Minute to 18 Months
Healthy volunteersNo

About this study

Hydrocephalus affects up to 2 out of every 500 births and results in long-term disability in up to 78% of those affected. The standard treatment of hydrocephalus is cerebrospinal fluid (CSF) diversion via placement of an invasive ventricular shunt to relieve elevated intracranial pressure (ICP). The clinical decision for CSF diversion is based on the ventricular size and clinical symptoms which are not robust indicators of brain health in neonatal hydrocephalus. The purpose of this study is to assess the safety and feasibility of performing brain contrast-enhanced ultrasound (CEUS) in neonates and infants with diagnosed and/or suspected hydrocephalus.

This description comes directly from the study's public registry record.

Talk to the study team

Misun Hwang, MD  ·  267-425-7110  ·  hwangm@chop.edu

Maria Mezher, MD  ·  267-425-5821  ·  mezherm@chop.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Children's Hospital of PhiladelphiaPhiladelphia, Pennsylvania, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06693752