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Omega-3 Supplementation for Tetraplegics With Poor Cholesterol Levels

Omega-3 Supplementation to Increase HDL-c Levels in Those With Tetraplegia

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01896037
Enrollment
21
Registered
2013-07-11
Start date
2013-07-31
Completion date
2017-03-28
Last updated
2017-05-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

High LDL-c, Low HDL-c, Quadraplegia, Spinal Cord Injury, Tetraplegia

Keywords

Spinal cord injury, Tetraplegia, Quadraplegia, Cholesterol, HDL-c, LDL-c, Omega-3 fatty acids

Brief summary

People with a spinal cord injury (SCI) characteristically have low levels of high-density lipoprotein-cholesterol (HDL-c; good cholesterol) and high levels of low-density lipoprotein-cholesterol (LDL-c; bad cholesterol), and are at a higher risk of developing cardiovascular health problems, such as heart disease, heart attack and stroke, than the able-bodied population. A common way for able-bodied people to improve their lipid profile is through exercise; however, SCI people, especially tetraplegics, are often unable to achieve and maintain a level of exercise needed to obtain these benefits. It is therefore clinically important to find an effective, safe and inexpensive method of increasing HDL-c levels in people with chronic tetraplegia. This study will investigate the effects of omega-3 fatty acid supplementation on the lipid profile of people with tetraplegia. The investigators hypothesize that 5 months of daily consumption of high doses of omega-3 fatty acids will increase plasma levels of HDL-c in those with tetraplegia, leading to decreased risk of cardiovascular health issues.

Interventions

DIETARY_SUPPLEMENTOmega-3 supplements

Daily omega-3 supplements of 600 mg EPA (Eicosapentaenoic acid) and 300 mg DHA (Docosahexaenoic acid) for 5 months.

Sponsors

The Association of Rehabilitation Medicine in Manitoba
CollaboratorUNKNOWN
University of Manitoba
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Having chronic tetraplegia (at least on year since injury) * 18 years or older * Having below normal fasting blood plasma levels of HDL-c (\<1 mmol/l)

Exclusion criteria

* Currently taking omega-3 supplements * Currently taking medications for abnormal cholesterol * Having a heart attack or stroke in the past one year

Design outcomes

Primary

MeasureTime frameDescription
Blood plasma levels of HDL-cholesterolMonth 5Change in blood plasma levels of HDL-cholesterol at month 5 compared to baseline levels

Secondary

MeasureTime frameDescription
Blood plasma levels of total cholesterolMonth 5Change in blood plasma levels of total cholesterol at month 5 compared to baseline levels

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026