I65.2 I65.0 I65.1 I66.0 I66.1 I66.2 I66.3 I66.4 I66.8 I65.8
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Age = 18 years 2. an at least mild-to-moderate (20-40% NASCET) Stenosis of one ore more extracranial brain supplying artery OR 3. any stenosis of an intracranial brain supplying artery OR 4. a revascularisation (either Operation or stenting) of an extracranial brain supplying artery in the past 5. written and informed consent of the participant
Exclusion criteria
Exclusion criteria: pregnant or breast-feeding patients
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. It shall be examined whether there is an association between the adherence to the "best medical therapy" and the cardio-vascular risk (assessment of cardio-vascular events as well as of the following surrogate parameters: high-sensitive CRP, total-, HDL- and LDL cholesterol, HbA1c, and sonographic progression of stenosis). | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. To identify factors that impair the implementation of BMT in a real world Setting. 2. The self-perception of patients concerning their vascular disease shall be examined. 3. To assess the Impact of BMT on cognition. | — |
Countries
Germany
Contacts
Klinik und Poliklinik für Neurologie, Universitätsklinikum Leipzig