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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02103842
Other study ID # 14-000639
Secondary ID
Status Completed
Phase Phase 1
First received March 18, 2014
Last updated December 22, 2015
Start date March 2014
Est. completion date July 2015

Study information

Verified date December 2015
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine how omega-3 fatty acids influence muscle protein metabolism and mitochondrial physiology in the context of human aging.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date July 2015
Est. primary completion date July 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- Age 18-35 or 65-85 years

Exclusion Criteria:

1. Current use of omega-3 nutritional supplements

2. Fasting plasma glucose =126 mg/dL

3. Active coronary artery disease

4. Participation in structured exercise (>3 times per week for 30 minutes or longer)

5. Smoking

6. Medications known to affect muscle metabolism (e.g., beta blockers, corticosteroids, tricyclic-antidepressants, benzodiazepines, opiates, barbiturates, anticoagulants)

7. Renal failure (serum creatinine > 1.5mg/dl)

8. Chronic active liver disease (Bilirubin > 17mmol/L, AST>144IU/L, or ALT>165IU/L)

9. Anti-coagulant therapy (warfarin/heparin)

10. INR >3

11. Use of systemic glucocorticoids

12. Chronic use of NSAIDS or aspirin

13. Pregnancy or breastfeeding

14. Alcohol consumption greater than 2 glasses/day

15. Hypothyroidism

16. Fish or shellfish allergy

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Omega-3 fatty acids


Locations

Country Name City State
United States Mayo Clinic Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Muscle protein synthesis Skeletal muscle protein synthesis will be measured from the rate of incorporation of infused amino acids measured by mass spectrometry. Baseline and following 4 months intervention No
Primary Change in Muscle mitochondrial function Mitochondrial function will be measured in isolated mitochondria by high-resolution respirometry. Baseline and following 4 months intervention No
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