- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07606001
Yellow Potatoes and Carotenoids
Effects of Yellow Flesh Potatoes on Carotenoid Status
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Wendy J Dahl, PhD
- Phone Number: 352-294-3707
- Email: wdahl@ufl.edu
Study Locations
-
-
Florida
-
Gainesville, Florida, United States, 32611
- University of Florida
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Adults ≥ 18 years of age; Able to provide written consent in English; Baseline Veggie Meter score of ≤ 300; Willing to adhere to study procedures;
Exclusion Criteria:
Baseline Veggie Meter score of >300; Potato allergy; Previously or currently being treated for intestinal disease, including irritable bowel syndrome, Crohn's disease, ulcerative colitis, celiac disease, or gastrointestinal cancer; Previous gastrointestinal surgery (e.g., gastric bypass, fundoplication, bowel resection); Current cancer treatment; Current pregnancy; Vegetarian diet; Elite athletes or long-distance runners.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Yellow-flesh potatoes
250 g of yellow-flesh potatoes
|
Participants will consume 250 g daily of yellow-flesh potatoes.
|
|
Placebo Comparator: White-flesh potatoes
250 g of white-flesh potatoes
|
Participants will consume 250 g daily of white-flesh potatoes.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Plasma zeaxanthin
Time Frame: 28 days
|
Plasma concentration of zeaxanthin
|
28 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Plasma lutein
Time Frame: 28 days
|
Plasma concentration of lutein
|
28 days
|
|
Skin carotenoid content
Time Frame: 28 days
|
Skin carotenoid content by reflection spectroscopy
|
28 days
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- IRB202600662
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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