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Study identifier: NCT07324421 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Comparison of Ultrasound Cerebral Perfusion Imaging With Routine Perfusion CT

Condition: Neuro ICU · Sub Arachnoid Hemorrhage · Neurological Complication  ·  Sponsor: Resolve Stroke

PhaseNA
Planned participants50
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The primary goal of neurocritical care is to prevent secondary brain injury, which worsens neurological outcomes. Because clinical monitoring is often insufficient due to the patient's condition and medical treatments, multimodal monitoring using biophysical, electrophysiological, and imaging data is essential. In patients with subarachnoid hemorrhage (SAH), the most frequent and severe complication is delayed cerebral ischemia, often linked to arterial vasospasm and potentially leading to infarction. Early diagnosis combines transcranial Doppler (TCD), sensitive to vasospasm, with perfusion CT (CTP), which measures cerebral perfusion; this approach guides therapy and improves prognosis. Ultrasound, especially when enhanced with contrast agents (CEUS), allows non-invasive, bedside, repeated visualization of cerebral blood flow and perfusion-even through the skull. Agents like SonoVue® help quantify perfusion using time-intensity curves. The study aims to assess whether cerebral perfusion measurements from the SYLVER device are equivalent to those from CTP in ICU or CCU patients.

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

Talk to the study team

Vivien Szabo, MD, PHD  ·  +33467336733  ·  v-szabo@chu-montpellier.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Centre Hospitalo-Universitaire Gui de ChauliacMontpellier, Herault, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT07324421