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Nutritional Supplement
Egg/Plant-Based Food Pairing for Nutritional Requirements
N/A
Waitlist Available
Research Sponsored by Ohio State University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 0, 3, 4.5, 6, 7.5, 9, 12, 24, 36, 48, 72 hours post-ingestion of spinach
Awards & highlights
Study Summary
This trial is testing whether eggs can help improve the nutrient absorption of vitamins E and K from plant foods.
Who is the study for?
This trial is for healthy adults with normal blood sugar, cholesterol levels, and body weight. Participants should not have gastrointestinal disorders or be taking medications that affect lipid or glucose metabolism. Smokers, vegetarians, pregnant women, heavy drinkers, those who changed their weight significantly recently or exercise extensively are excluded.Check my eligibility
What is being tested?
The study tests if eating eggs along with deuterium-labeled spinach increases the body's absorption of vitamins E and K from the spinach compared to eating spinach alone or with vegetable oil. It will measure how well these nutrients enter the bloodstream when paired with different foods.See study design
What are the potential side effects?
Since this trial involves common foods like eggs and spinach without any experimental drugs involved, side effects are expected to be minimal. However, individuals may experience typical food-related reactions based on personal sensitivities.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 0, 3, 4.5, 6, 7.5, 9, 12, 24, 36, 48, 72 hours post-ingestion of spinach
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~0, 3, 4.5, 6, 7.5, 9, 12, 24, 36, 48, 72 hours post-ingestion of spinach
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Estimated Absorption (%Dose) of Vitamin E
Estimated Absorption (%Dose) of Vitamin K
Vitamin E Bioavailability
+3 moreSecondary outcome measures
Chylomicron Vitamin E
Chylomicron Vitamin K
Elimination Rate of Vitamin E
+3 moreOther outcome measures
Malondialdehyde
Vitamin C
Trial Design
4Treatment groups
Experimental Treatment
Group I: Zero hard-boiled eggExperimental Treatment1 Intervention
Deuterium-labeled spinach containing 2 mg αT and 500 ug PQ will be ingested alone prior to the 72-h pharmacokinetics trial.
Group II: Vegetable oilExperimental Treatment1 Intervention
Deuterium-labeled spinach containing 2 mg αT and 500 ug PQ will be ingested with vegetable oil (9.6 g fat) prior to the 72-h pharmacokinetics trial.
Group III: Two hard-boiled eggsExperimental Treatment1 Intervention
Deuterium-labeled spinach containing 2 mg αT and 500 ug PQ will be ingested with two whole eggs (9.6 g fat) prior to the 72-h pharmacokinetics trial.
Group IV: Two egg whitesExperimental Treatment1 Intervention
Deuterium-labeled spinach containing 2 mg αT and 500 ug PQ will be ingested with two egg whites (0 g fat) prior to the 72-h pharmacokinetics trial.
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Who is running the clinical trial?
Ohio State UniversityLead Sponsor
830 Previous Clinical Trials
505,610 Total Patients Enrolled
1 Trials studying Nutritional Requirements
10 Patients Enrolled for Nutritional Requirements
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Eligibility Criteria:
This trial includes the following eligibility criteria:- My weight has changed by more than 2 kg in the last month.My BMI is between 19 and 25.I consume more than 2 alcoholic drinks daily.I have no history of stomach or intestine problems.I follow a vegetarian diet.I am not taking medication that affects my cholesterol or blood sugar levels.I am allergic to eggs.I haven't taken dietary supplements for over a month.I engage in physical activities like walking or cycling for more than 7 hours a week.
Research Study Groups:
This trial has the following groups:- Group 1: Zero hard-boiled egg
- Group 2: Two hard-boiled eggs
- Group 3: Vegetable oil
- Group 4: Two egg whites
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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