CClinicalTrials.gg
CompletedNCT01432210Updated Sep 30, 2016

Provitamin A Absorption and Conversion With Avocados

An interventional study of Post-prandial Feeding Study in Healthy, sponsored by Ohio State University. Completed at 1 site in United States. Open to participants aged 18 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-09-30.

Sponsored by Ohio State University · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
24
Allocation
Randomized
Ages
18 Years to 70 Years
Sex
All
01

Study summary

Vitamin A is necessary in the human diet. The form of vitamin A found in fruits and vegetables is not "active" and must be converted to the active form in the human body. However, information on the ability of humans to absorb and convert vitamin A to the active form is still lacking. In this study, the investigators will observe the absorption and conversion of vitamin A from orange tomato sauce and/or carrots after a meal with fat (from avocado fruit) and a meal without fat. The investigators will also test whether eating these foods might protect the blood against damage that could lead to heart disease.

Read the detailed description

The primary objective of this study will be to demonstrate that adding avocados to a carotene rich meal will promote the absorption of provitamin A carotenoids and enhance the delivery of greater quantities of vitamin A. This objective will be accomplished by quantitation of the immediate post-prandial plasma concentrations of parent carotenoids and vitamin A metabolites after subjects consume a meal with or without avocado in combination with a serving of tomato sauce (containing nutritionally relevant amounts of beta-carotene) or carrots.

The secondary objective of this study will be to determine if higher levels of carotenoids and other antioxidants transported in the bloodstream will have a protective role in promoting cardiovascular health. This objective will be accomplished by testing the oxidation capacity of lipoprotein fractions before and after meal supplementation.

02

Conditions studied

  • Healthy

Keywords

  • post-prandial absorption
  • provitamin A carotenoids
  • vitamin A
  • avocado
  • tomato
  • carrot
03

In context

Lead sponsor

Ohio State University is the lead sponsor of 640 studies on the registry; 144 are open to participants now.

Of its 60 completed or terminated interventional studies of FDA-regulated products, 45 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Total cholesterol (140 to 200 mg/dL)
  • BMI 17 to 30
  • Age 18-70 years

Exclusion criteria

Exclusion Criteria:

  • Lactating, pregnant, or plan to be pregnant during study
  • Tobacco use (cigarettes or chewing tobacco)
  • Metabolic disease
  • Malabsorption disorders
  • History of cancer, esophageal, gastric, or intestinal ulcers
  • History of liver or kidney insufficiency or failure
  • Allergies to tomatoes or tomato products
  • Allergies to carrots
  • Allergies to avocados
  • Obesity (BMI>30)
  • Hypercholesterolemia (total cholesterol> 200mg/dL)
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
24 participants (actual)

Study arms

  • Other
    Tomato Meal

    A tomato meal will be fed with and without avocado.

    Other: Post-prandial Feeding Study

  • Other
    Carrot Meal

    A carrot meal will be fed with and without avocado.

    Other: Post-prandial Feeding Study

Interventions

  • OtherPost-prandial Feeding Study
06

What researchers measure

Primary outcomes

  1. Post-prandial levels of provitamin A and vitamin A

    The absorption of and conversion of provitamin A carotenoids into vitamin A will be measured after the consumption of a carotenoid-rich meal. The meal will be served both with and without avocado as a source of lipid.

    Time frame: Nine post-prandial blood samples will be taken over twelve hours

Secondary outcomes

  1. post-prandial antioxidant status of blood

    The ability of a carotenoid-rich meal to reduce the susceptibility of blood lipoproteins to oxidative stress will be tested. A modified trolox equivalent antioxidant capacity (TEAC) assay will be used.

    Time frame: comparing baseline vs. 5 hour status

07

Study locations

1 site
  • The Ohio State University Clinical Research Center
    Columbus, Ohio 43210, United States
08

References and documents

Publications

  • Cooperstone JL, Goetz HJ, Riedl KM, Harrison EH, Schwartz SJ, Kopec RE. Relative contribution of alpha-carotene to postprandial vitamin A concentrations in healthy humans after carrot consumption. Am J Clin Nutr. 2017 Jul;106(1):59-66. doi: 10.3945/ajcn.116.150821. Epub 2017 May 17. PubMed 28515067 ↗
  • Kopec RE, Cooperstone JL, Schweiggert RM, Young GS, Harrison EH, Francis DM, Clinton SK, Schwartz SJ. Avocado consumption enhances human postprandial provitamin A absorption and conversion from a novel high-beta-carotene tomato sauce and from carrots. J Nutr. 2014 Aug;144(8):1158-66. doi: 10.3945/jn.113.187674. Epub 2014 Jun 4. PubMed 24899156 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 30, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01432210
Lead sponsor
Ohio State University
Collaborators
Hass Avocado Board
Responsible party
Jessica Cooperstone (Research Scientist, Ohio State University) — Principal investigator
First posted
Sep 12, 2011
Start date
Sep 2011
Primary completion
Jan 2012
Completion
Mar 2012
Last update
Sep 30, 2016

Study contacts

Steven J Schwartz, Ph.D.
principal investigator · Ohio State University

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Sep 2016. You cannot join it, but the record below documents what was studied.

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