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Clinical Trial Summary

This is a prospective, multicenter, single-arm, open-label, national Post-Market Clinical Follow-up study to collect comprehensive information on technical and clinical success and safety of the use of APERIO® Hybrid(17/21) Thrombectomy Device in clinical practice. APERIO® Hybrid(17/21) Thrombectomy Device will be used within its approved indication.


Clinical Trial Description

German APERIO® Hybrid Post- Market Clinical Follow-up Study APERIO® Hybrid PMCF Study- Thrombectomy device for flow restoration in vessels of patients experiencing acute ischemic stroke Study Type: prospective, multicenter, single-armed, open-label Participants: 8 participating centers in Germany PI: Dr. Christian Mathys, Evangelisches Krankenhaus Oldenburg, Germany Estimated Enrolment: 190 patients treated with APERIO® HYBRID(17/21) Thrombectomy Device as a result of an acute stroke Follow up: 3 months Estimated Final Assessment: Mid to End of 2023 ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04457479
Study type Observational [Patient Registry]
Source Acandis GmbH
Contact
Status Completed
Phase
Start date November 2, 2020
Completion date June 30, 2023

See also
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