Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
60 participants
INTERVENTIONAL
2022-07-11
2024-09-01
Brief Summary
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A total of 60 adult diabetic male and female participants will be recruited to take part in this double-blinded, randomized, placebo-controlled, parallel trial. Participants will be randomly assigned to include two DHA and lutein enriched eggs or regular eggs into their usual diet for 6 weeks. At the beginning and end of the trial, a variety of measures will be analyzed including blood lipid parameters, carotenoid status, anthropometrics, arterial stiffness, advanced glycated end products, macular pigment optical density and electroretinography. These measures will aid in determining whether enriched egg consumption can safely improve retina function, while not adversely effecting body composition and cardiovascular risk factors in individuals with diabetes. The results of this study will contribute to the development of valuable prevention strategies for eye health in individuals with diabetes, thereby improving their quality of life.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
DOUBLE
Study Groups
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Enriched Egg Group
Participants will consume 2 medium sized docosahexaenoic acid and lutein enriched eggs daily (at least 5 days per week) for 6 weeks.
Docosahexaenoic Acid and Lutein Enriched Eggs
Consumption of 2 docosahexaenoic acid and lutein enriched eggs daily (at least 5 days our week) for 6 weeks
Regular Egg Group
Participants will consume 2 medium sized non-enriched eggs daily (at least 5 days per week) for 6 weeks.
Regular Eggs
Consumption of 2 non enriched eggs daily (at least 5 days our week) for 6 weeks
Interventions
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Docosahexaenoic Acid and Lutein Enriched Eggs
Consumption of 2 docosahexaenoic acid and lutein enriched eggs daily (at least 5 days our week) for 6 weeks
Regular Eggs
Consumption of 2 non enriched eggs daily (at least 5 days our week) for 6 weeks
Eligibility Criteria
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Inclusion Criteria
* Individuals diagnosed with Type 2 diabetes
* Individuals taking oral hypoglycemic medications (sulfonylureas, meglitinides, biguanides, thiazolidinediones etc.)
* Individuals with a fasting plasma glucose of ≥7.0 mmol/L or glycated hemoglobin (A1C) of ≥6.5%. (these values are based on the Canadian Diabetes Association and are predictors of the development of diabetic retinopathy)
Exclusion Criteria
* Individuals with eye disease (cataracts, glaucoma, age-related macular degeneration, retinitis pigmentosa, optic atrophy, and eye malformation etc.)
* Individuals with Alzheimer's, dementia or other mental cognitive diseases
* Individuals with Type 1 diabetes
* Individuals taking insulin
* Individuals diagnosed with cancer or anemia
* Pregnant women
19 Years
ALL
Yes
Sponsors
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Egg Farmers of Canada
UNKNOWN
University of Manitoba
OTHER
Responsible Party
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Principal Investigators
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Miyoung Suh, RD, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Manitoba
Locations
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Asper Clinical Research Institute
Winnipeg, Manitoba, Canada
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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B2020:007
Identifier Type: -
Identifier Source: org_study_id
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