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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01813006
Other study ID # 2011/899(REK)
Secondary ID 2012-000505-68
Status Completed
Phase Phase 3
First received
Last updated
Start date March 2013
Est. completion date December 2017

Study information

Verified date March 2013
Source Nordlandssykehuset HF
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Background

Familial hypercholesterolemia (FH) is an inherited disease in which the level of bad cholesterol (LDL-cholesterol) is increased, leading to an increase in coronary heart disease even if adequately treated with cholesterol lowering medication (statins). Polyunsaturated fatty acids (PUFA) including omega-3 is known to affect the risk for coronary disease, however its effect on patients with FH is not known.

The purpose of the study is to assess the effect of PUFA on patients with FH, with regard to inflammation measured in the blood and the effect on the blood vessels`ability to relax (endothelial function) by means of tonometry.

Hypothesis

Treatment with 4 grams of PUFA a day for 4 months will lead to an improvement in the endothelial function, and the treatment will also lead to a decrease in in several markers of inflammation and in lipids in the blood.


Recruitment information / eligibility

Status Completed
Enrollment 34
Est. completion date December 2017
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- documented familial hypercholesterolemia

- age 18-60 years

- on statin treatment for at least 12 months

Exclusion Criteria:

- pregnancy or planned pregnancy

- breast feeding

- cancer

- non-compliance

- PUFA/omega-3 < 3 months before inclusion

Study Design


Intervention

Drug:
Omega-3

placebo


Locations

Country Name City State
Norway Division of Internal Medicine, Nordland Hospital Bodø

Sponsors (2)

Lead Sponsor Collaborator
Nordlandssykehuset HF Pronova BioPharma

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Other Lipid parameters Different fractions of lipids in the blood including LDL-cholesterol, HDL cholesterol, triglycerides and their subfractions Baseline
Other Lipid parameters Different fractions of lipids in the blood including LDL-cholesterol, HDL cholesterol, triglycerides and their subfractions 3 months
Other Lipid parameters Different fractions of lipids in the blood including LDL-cholesterol, HDL cholesterol, triglycerides and their subfractions 6 months
Other Lipid parameters Different fractions of lipids in the blood including LDL-cholesterol, HDL cholesterol, triglycerides and their subfractions 9 months
Primary Reactive Hyperemia Index (RHI) Reactive Hyperemia Index (RHI) is a measure for endothelial function by means of tonometry Baseline
Primary Reactive Hyperemia Index (RHI) Measure of endothelial function 3 months
Primary Reactive Hyperemia Index (RHI) Measure of endothelial function 6 months
Primary Reactive Hyperemia Index (RHI) Measure of endothelial function 9 months
Secondary Markers of inflammation Serological markers of inflammation including cytokines, C-reactive protein (CRP) and complement factors Baseline
Secondary Inflammatory markers Serological markers of inflammation including cytokines, CRP and complement factors 3 months
Secondary Inflammatory markers Serological markers of inflammation including cytokines, CRP and complement factors 6 months
Secondary Inflammatory markers Serological markers of inflammation including cytokines, CRP and complement factors 9 months
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