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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02957188
Other study ID # 13C EPA and 13C AA metabolism
Secondary ID
Status Completed
Phase N/A
First received October 24, 2016
Last updated November 2, 2016
Start date August 2015
Est. completion date August 2016

Study information

Verified date November 2016
Source Université de Sherbrooke
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine the kinetics of 13C-eicosapentaenoic acid (EPA) and 13C-arachidonic acid (AA) in young and older participants


Recruitment information / eligibility

Status Completed
Enrollment 13
Est. completion date August 2016
Est. primary completion date July 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years and older
Eligibility Inclusion Criteria:

- six young (18-30 y old) and six older (= 70 y old)

- healthy non medicated participants.

Exclusion Criteria:

- Tobacco,

- malnutrition (assessed from blood albumin, haemoglobin and lipids), -

- participants taking an EPA+DHA supplements or consuming more than 2 fish meals per week,

- severe gastro-intestinal problems,

- medication for diabetes,

- thyroid disease,

- renal failure,

- cancer,

- psychiatric difficulties or depression,

- cardiovascular disease,

- glucose intolerance (>8 mmol/L in fasted samples)

- chronic immune condition or inflammation (CRP > 10 mg/l, white cell count),

- recent major surgery or cardiac event,

- dementia,

- ongoing or past severe drug or alcohol abuse,

- ongoing or past intensive physical training.

Study Design

Observational Model: Case-Crossover, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Intervention

Other:
13C eicosapentaenoic acid and 13C arachidonic acid
Each participant orally consumed a single oral dose of 35 mg of 13C-EPA, and after the wash-out, a 50 mg dose of 13C-AA.

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Université de Sherbrooke Healthy Aging Research Network

Outcome

Type Measure Description Time frame Safety issue
Primary Kinetics of 13C-EPA and 13C-AA Plasma incorporation of 13C-EPA or 13C-AA was measured from the area under the curve in young and older participants over 28 days post-dose No
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