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Clinical Trial Summary

This study will be conducted in up to 10 hospitals in Europe, up to 75 patients will be enrolled. The purpose of the study is to evaluate any debris that may be captured in the inline filter of the MICHI(TM) Neuroprotection System with Filter (NPS+f) during its use in a transcarotid stenting procedure. The MICHI NPS+f is an embolic protection device that uses reverse flow to protect the brain during stenting of the Internal Carotid Artery. It is CE marked and is used in routine practice for the purpose of this study.


Clinical Trial Description

n/a


Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT01877174
Study type Observational
Source Silk Road Medical
Contact
Status Completed
Phase N/A
Start date May 2013
Completion date October 2013

See also
  Status Clinical Trial Phase
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Completed NCT02398734 - SONOlysis in Prevention of Brain InfaRctions During Internal Carotid Endarterectomy N/A
Completed NCT01591005 - SONOlysis in Prevention of Brain Infarctions dUring Carotid Stenting and caroTid EndaRterectomy Phase 3
Completed NCT02794974 - Ultrasound-guided Intermediate Cervical Plexus Block N/A
Recruiting NCT03121209 - Carotid Revascularization and Medical Management for Asymptomatic Carotid Stenosis Trial - Hemodynamics (CREST-H) Phase 3
Recruiting NCT05260229 - The Observation About the Effects of Internal Carotid Artery Stenosis on Fundus Vessels and the Changes of Fundus Vessels After Interventional Therapy