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Clinical trial

Post-Approval Study - Post-Market Surveillance Study to Evaluate the Long-Term Safety and Effectiveness of the LVIS® Device

NCT05453240 is registered in ClinicalTrials.gov with Microvention-Terumo, Inc. as lead sponsor.

NCT NCT05453240
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Registry record

As filed in ClinicalTrials.gov.

Title
Post-Approval Study - Post-Market Surveillance Study to Evaluate the Long-Term Safety and Effectiveness of the LVIS® Device
Lead sponsor
Microvention-Terumo, Inc.
Phase
Observational
Overall status
Enrolling by invitation
Start date
November 17, 2020
Completion date
January 1, 2026
Enrollment
250 (estimated)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

intracranial aneurysms