hypercholesterolemia
Conditions
Interventions
None listed
Sponsors
LIVES Study Extension advisory committee
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients who have been included in LIVES study
Exclusion criteria
Exclusion criteria: No written formed informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Myocardial infarction, intervention due to angina, angina requiring hospitalization 2. Cerebral vascular events(infarction, hemorrhage, subarachnoid hemorrhage) 3. Sudden death | — |
Countries
Japan
Contacts
Public ContactMitsuyoshi Urashima
Jikei University School of Medicine Division of Molecular Epidemiology
Outcome results
None listed