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Bioavailability of Encapsulated Omega-3 Fatty Acids

U

United States Army Research Institute of Environmental Medicine

Status

Completed

Conditions

Bioavailability of Omega-3s in Military Rations

Treatments

Dietary Supplement: encapsulated 600 mg EPA/DHA

Study type

Interventional

Funder types

Other U.S. Federal agency
Other

Identifiers

NCT01940679
13-13-H

Details and patient eligibility

About

Omega-3 fatty acids (n-3s), particularly eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), have anti-inflammatory properties and other documented beneficial health effects that could warrant n-3 fortification of combat rations. However, military combat rations must meet rigorous shelf-stability guidelines (e.g.,, 3 years at 80°F or 6 months at 100°F), which is problematic for natural food sources of n-3s (e.g., oil and fish), which degrade when exposed to high temperatures and prolonged shelf-storage. Encapsulation, e.g., coating freeze dried n-3s with gelatin, can prevent this degradation, and Natick Soldier Research, Development and Engineering Center's (NSRDEC) Combat Feeding Directorate used encapsulated n-3 technology to produce n-3 enriched ration items that withstand environmental stressors and meet shelf-life specifications for military rations. However, the bioavailability of the encapsulated n-3s in these rations is unknown, particularly when they are incorporated into high-protein food items and exposed to high temperatures and prolonged storage. In this randomized, cross-over study, civilian and/or military personnel will be asked to consume: 1) a high protein food item enriched with encapsulated n-3s (600 mg) and previously stored for 6 months at 100°F; 2) a low-protein food item enriched with encapsulated n-3s (600 mg) and previously stored for 6 months at 100°F; 3) a high protein food item with encapsulated n-3s (600 mg) that was not subjected to high-temperature and prolonged storage; and, 4) a low-protein food item with encapsulated n-3s (600 mg) that was not subjected to high temperature and prolonged storage. Serial blood sampling to measure acute changes in the circulating fatty acid profile will occur in the hour before and 6 hours after consumption of each ration component. The only known risks, which this study presents to participants, are those associated with venous catheter placement. The results will help military ration developers determine the ration components best suited for n-3 fortification.

Enrollment

14 estimated patients

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • between 18 and 45 years old
  • leave status and have approval from your supervisor (for DoD Civilians)

Exclusion criteria

  • under the age of 18 or over the age of 45
  • bleeding disorder (von Willebrand disease, hemophilia) or taking medications that impair ability to stop bleeding (heparin)
  • consumed ≥1 serving (equivalent to a deck of cards) of salmon, herring, mackerel, anchovies, sardines, halibut or tuna or omega-3 enriched eggs per week over the previous past month
  • regularly consume dietary supplements (for example, capsules) containing omega-3 fatty acids

Trial design

14 participants in 4 patient groups

Fresh meat stick
Experimental group
Description:
Fresh meat stick w/ encapsulated 600 mg EPA/DHA; product frozen immediately after production.
Treatment:
Dietary Supplement: encapsulated 600 mg EPA/DHA
Stored meat stick
Experimental group
Description:
Stored meat stick with encapsulated 600 mg EPA/DHA; stored at 100F for 3 months after production
Treatment:
Dietary Supplement: encapsulated 600 mg EPA/DHA
Fresh pound cake
Experimental group
Description:
Fresh pound cake w/ encapsulated 600 mg EPA/DHA; product frozen immediately after production.
Treatment:
Dietary Supplement: encapsulated 600 mg EPA/DHA
Stored pound cake
Experimental group
Description:
Stored pound cake with encapsulated 600 mg EPA/DHA; stored at 100F for 3 months after production.
Treatment:
Dietary Supplement: encapsulated 600 mg EPA/DHA

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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