Assessing the Effects of Corn and Avocado Oils on the Cardiometabolic Risk Factor Profile

Part of paid clinical trials in Addison, Illinois.

Sponsor
Midwest Center for Metabolic and Cardiovascular Research
Study ID
NCT07514663
Status
Recruiting
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Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - 74 Years
Healthy Volunteers
Accepted

Interventions

  • corn oil — OTHER
    Corn oil will be provided in yogurt, rolls and muffins throughout the study period.
  • Avocado Oil — OTHER
    Avocado oil will be provided in yogurt, rolls and muffins throughout the study period.

Study Details

The goal of this clinical trial is to assess the effects of corn and avocado oils as part of controlled feeding diets on the cardiometabolic risk factor profile in men and women with mild-to-moderately elevated levels of non-high-density lipoprotein cholesterol (non-HDL-C). Participants will be asked to consume the controlled feeding diet for two separate 21 day conditions, and will consume their regular diet for a 21 day washout period between the two conditions. Additionally, participants will be asked to come into the clinic on 7 different occasions, including one screening visit (visit 1, -7 days), one baseline visit (visit 2, day 0), two visits during each 21-d diet condition (visits 3 \& 6, day 19 and visits 4 \& 7, day 21), and a visit at the conclusion of the washout phase/start of the second diet condition (visit 5, day 0).

Key Dates

Start date
Apr 10, 2026
Status verified
Apr 2026
Primary completion
Sep 30, 2026
Completion
Sep 30, 2026

Study Design

Enrollment
54 participants (estimated)
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER

Arms

  • Experimental: Corn Oil
    Corn oil (4 tablespoons/d) will be provided in 3 servings of study products per day (yogurt, dinner roll, and muffin).
  • Active Comparator: Avocado Oil
    Avocado oil (4 tablespoons/d) will be provided in 3 servings of study products per day (yogurt, dinner roll, and muffin).

Primary Outcome Measure

Non-high density lipoprotein cholesterol (non-HDL-C) [ Time Frame: Baseline (day 0) to end of each condition (day 21) ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Biofortis Clinical ResearchAddisonIllinois60101
Gina Castiglione-Berg
[email protected]
(630) 617-2000

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By research site
Biofortis Clinical Research· Addison, IL

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