cervical carotid artery
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients who plan to undergo carotid endoarterectomy (CEA) and meet following criteria. A)Patients who have misery perfusion on preoperative examinations and give consent. B) Control group patients who had misery perfusion and underwent CEA without using intraluminal shunt between 2020/7/1 to 2025/6/30.
Exclusion criteria
Exclusion criteria: A) 1. Patients who have thinner diameter of outer diameter of intraluminal shunt tube (3mm) 2. Patients who lack required data. B) 1. Patients who reject to be included the study 2. Patients that intraluminal shunt could not be implanted 3. Patients who lack required data.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of hyperperfusion for up to 1-7 days after surgeries | — |
Secondary
| Measure | Time frame |
|---|---|
| Analysis of relation between findings of intraoperative monitoring and post-operative hyperperfusion | — |
Countries
Japan
Contacts
Iwate Medical University Hospital Neurosurgery