Obesity Clinical Trial
Official title:
Whole Egg Intake and the Mediterranean Diet
NCT number | NCT02737293 |
Other study ID # | GFHNRC147 |
Secondary ID | |
Status | Terminated |
Phase | N/A |
First received | |
Last updated | |
Start date | April 2016 |
Est. completion date | March 25, 2020 |
Verified date | August 2022 |
Source | USDA Grand Forks Human Nutrition Research Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This project will evaluate the daily intake of whole eggs in the Mediterranean Diet (Med Diet). Cholesterol levels are normally related to cardiovascular disease (CVD) risk. Dietary fat and the total diet makeup are well known modifiers of CVD risk. The Med Diet has been shown to decrease blood lipids (fats) and reduce inflammation. Cholesterol intake from eggs may not be as bad as once thought and, in fact, may help to improve the blood lipid (fat) levels. This study is being done to test how the addition of eggs to a Med Diet affects blood lipids and other risk markers for CVD.
Status | Terminated |
Enrollment | 33 |
Est. completion date | March 25, 2020 |
Est. primary completion date | March 25, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 20 Years to 75 Years |
Eligibility | Inclusion Criteria: - Willingness to comply with the demands of the experimental protocol - Not performing vigorous exercise >2 times per week - BMI 25-39.9 kg/m2 - Non-nicotine-using Exclusion Criteria: - Have an egg allergy - Have diabetes - Have high triglyceride levels - Have uncontrolled high blood pressure - Have used tobacco products or nicotine in any form including snuff, pills and patches, or e-cigarettes in the previous 6 months - Use prescription medications or over-the-counter lipid lowering drugs (such as statins) or anti-inflammatory medications (such as aspirin, ibuprofen or Aleve) on a regular basis - Take omega 3 supplements, plant sterols or sterol esters - Are pregnant or lactating - Have been diagnosed with an eating disorder - Inability to give consent - Unwillingness or inability to consume the treatment diets |
Country | Name | City | State |
---|---|---|---|
United States | USDA Grand Forks Human Nutrition Research Center | Grand Forks | North Dakota |
Lead Sponsor | Collaborator |
---|---|
USDA Grand Forks Human Nutrition Research Center | Egg Nutrition Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in lipoprotein metabolism | Assess lipid metabolism response to the intervention. | baseline and 4 weeks | |
Secondary | Change in inflammatory markers | Determine inflammatory marker response to the intervention. | baseline and 4 weeks |
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