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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01896037
Other study ID # HDL2013
Secondary ID
Status Completed
Phase Phase 4
First received July 5, 2013
Last updated May 3, 2017
Start date July 2013
Est. completion date March 28, 2017

Study information

Verified date May 2017
Source University of Manitoba
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 21
Est. completion date March 28, 2017
Est. primary completion date January 28, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Intervention

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

Locations

Country Name City State
Canada Health Sciences Centre Winnipeg Manitoba

Sponsors (2)

Lead Sponsor Collaborator
University of Manitoba The Association of Rehabilitation Medicine in Manitoba

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Blood plasma levels of HDL-cholesterol Change in blood plasma levels of HDL-cholesterol at month 5 compared to baseline levels Month 5
Secondary Blood plasma levels of total cholesterol Change in blood plasma levels of total cholesterol at month 5 compared to baseline levels Month 5
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