carotid artery stenosis
Conditions
Interventions
None listed
Sponsors
Graduate School of Medicine, Gifu University
Ichinomiya West Hospital Ube Kosan Central Hospital Kizawa Memorial Hospital Toki Municipal Hospital Hyogo College of Medicine Hiroshima University Hospital Fukuroi Municipal Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Patient scheduled for CAS from Oct. 1st, 2011 to Sept. 30th, 2013 2) Patients can receive MR plaque imaging before CAS 3) Patient who signed an informed consent form
Exclusion criteria
Exclusion criteria: Patients who are judged as inappropriate to participate in this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Major adverse event (MAE) including any stroke, myocardial infarction, or death within 90 (+/-10) days after CAS | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) Relationship between MR plaque imaging and MAEs or the number of newly appeared high intensity signals 1-3 days after CAS 2) Relationship between method of cerebral protection and MAEs or the number of newly appeared high intensity signals 1-3 days after CAS 3) Relationship between laboratory data and MAEs or the number of newly appeared high intensity signals 1-3 days after CAS 4) Relationship between stent type and MAEs or the number of newly appeared high intensity signals 1-3 days after CAS | — |
Countries
Japan
Outcome results
None listed