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Amnis Therapeutics Thrombectomy Device-First in Man (FIM) Safety and Performance Study

Ischemic Stroke Clinical Trial

Official title:
Amnis Therapeutics Thrombectomy Device-First in Man (FIM) Safety and Performance Study

Clinical Trial Summary

Prospective, single-arm, open label, Safety and Performance clinical investigation.

Clinical Trial Description

The Amnis Thrombectomy Device is intended to restore blood flow by removing thrombus from intracranial vessels in patients experiencing ischemic stroke. Pre-CE mark clinical investigation. Population will be subjects with documented untreated, acute ischemic stroke with large vessel occlusion. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02994563
Study type Interventional
Source Amnis Therapeutics
Contact
Status Terminated
Phase N/A
Start date October 7, 2019
Completion date March 1, 2021
View Details
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