Transcranial Ultrasound Via Sonolucent Cranioplasty After Minimally Invasive Intracerebral Hemorrhage Evacuation
Recruiting
N/A
Interventional Study
Transcranial Ultrasound With Sonolucent Cranioplasty
TUSC
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Diagnostic
- Participants needed
- 25 (estimated)
- Sponsor
- Icahn School of Medicine at Mount Sinai · Other
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About This Trial
Postoperative rebleeding is a major limitation of surgical evacuation for intracerebral hemorrhage (ICH). While computed tomography (CT) is the standard of care for postoperative hematoma cavity monitoring, CT requires significant physical and financial costs. Studies have demonstrated varying degrees of efficacy when using transcranial ultrasound to measure ICH volume. Recently, synthetic implant…
Trial Locations
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Eligibility Criteria
Inclusion criteria:
* Presence of spontaneous supratentorial ICH ≥20 mL
* Age ≥18 years
* National Institute of Health Stroke Scale (NIHSS) score ≥6
* GCS score 5-15 at presentation
* Undergoing minimally invasive intracerebral hemorrhage evacuation with sonolucent cranioplasty or hemicraniectomy w…
Contacts