familial elevated cholesterol familial hypercholesterolemia
Conditions
Interventions
None listed
Sponsors
Academisch Medisch Centrum
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Those who participated in the LIPIDS trial and their non-affected brothers or sisters
Exclusion criteria
Exclusion criteria: None
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main endpoint will be the difference in IMT between FH patients and their non-affected siblings after 10 years follow-up. | — |
Secondary
| Measure | Time frame |
|---|---|
| Furthermore, we will investigate change in IMT after 10 years follow-up for various treatment durations and intensities. The occurrence of adverse events and growth and sexual development will be described and compared to healthy siblings. We will also investigate psychological effects. | — |
Countries
Netherlands
Outcome results
None listed