An EFS to Evaluate the CGuard Prime™ Carotid Stent in Acute Ischemic Stroke
Running, not enrolling · Not applicable
Conditions studied: Acute Ischemic Stroke
In brief
The Jacobs Institute is conducting a Sponsor Investigator study of patients ≥ 18 years to establish safety and preliminary effectiveness in treating extracranial stenosis with the CGuard Prime™ Carotid Stent in the setting as an acute ischemic stroke.
Key facts
- Study ID
- NCT06447116
- Run by
- Jacobs institute
- People needed
- 15
- Starts
- 2025-01-01
- Expected to finish
- 2026-12-31
- Last updated by the study team
- 2026-03-05
Who can join
Age: 18 and older, up to 90. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients ≥18-year-old; Carotid stenosis with at least ≥ 50% stenosis; National Institute of Health Stroke Scale (NIHSS) >/=6; and evidence of large vessel occlusion (LVO) in the anterior circulation (i.e., intracranial internal carotid artery, M1 and proximal M2) by computed tomography angiography (CTA).
You may not qualify if…
- Cannot provide consent or legally authorized representative not available to provide consent. Evidence of intracranial hemorrhage on non-contrast CT or MRI; ASPECTS<6; and any contraindication to dual antiplatelet therapy.
Where it is running
- Jacobs Institute — Buffalo, New York, United States
Full record on ClinicalTrials.gov
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