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Clinical Trial Summary

Compare the safety and effectiveness of pRESET to Solitaire in the treatment of stroke related to large vessel occlusion


Clinical Trial Description

To determine the safety and effectiveness of pRESET for the treatment of acute ischemic stroke within 8 hours of symptom onset (defined as time patient was last seen well) due to large vessel occlusion and to compare safety and effectiveness to the predicate device, Solitaireā„¢ Platinum revascularization device ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03994822
Study type Interventional
Source phenox Inc.
Contact
Status Completed
Phase N/A
Start date October 4, 2019
Completion date May 12, 2022

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