Comparison of Ultrasound Cerebral Perfusion Imaging With Routine Perfusion CT

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorResolve Stroke

About this trial

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.

Eligibility criteria

Qualifiers

Patient ≥ 18 years old

Patient Informed Consent, or from his/her relative if the patient is not conscious and able to consent

Admission to ICU or CCU with indication to perform at least one CTP

Affiliated with or benefiting from a social security scheme

Disqualifiers

Guardianship, curatorship or any deprivation of liberty by judicial or administrative decision

Pregnant or breast-feeding women

Known contra-indication or hypersensitivity to SonoVue® (to sulfur hexafluoride microbubbles or to one of its excipients such as polyethylene glycol (PEG))

Right-to-left shunts

Trial design

Treatments tested in this trial

  • Ultrasound contrast agent (Contrast-enhanced ultrasound)

Treatment groups

50 Participants
are divided into 1 treatment group

Sponsors and collaborators