Ischemic Stroke Clinical Trial
Official title:
Delphi Early Feasibility Study (DELPHI EFS)
An early feasibility study to evaluate the safety and first pass effect technical assessment of Delphi Revascularization Device for clot retrieval in Anterior circulation ischemic stroke in the intracranial ICA, MCA M1 and proximal dominant MCA M2, up to 8hrs of symptom onset or Last Known Well (LKW).
The Delphi Revascularization Device is a stent retriever that has electrical current applied and is a combination of the Solitaire™ X Revascularization Device and an accessory device to apply the electrical current, the ADD. There is bench evidence that electrical current changes the properties of the clot, which can improve clot adhesion and neurothrombectomy, and an improved rate of first pass success. The small electric current is intended to polymerize the proteins in the clot and cause better clot engagement and this in turn would have better first pass effect, lower chances of safety issues and better long-term clinical outcomes ;
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