Davis, CANCT05545865Now EnrollingIRB Ready

Cardiovascular Diseases Clinical Trial in Davis, CA

Access cutting-edge cardiovascular diseases treatment through this clinical trial at a research site in Davis. Study-provided care at no cost to qualified participants.

Sponsored by University of California, Davis

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Expert Care in Davis

Access cardiovascular diseases specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related cardiovascular diseases treatment provided free

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Check if you qualify for this cardiovascular diseases clinical trial in Davis, CA

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Davis

    Convenient for CA residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Davis site if eligible
  4. 4Begin participation

About This Cardiovascular Diseases Study in Davis

This study aims to obtain data on the potential influence of Vine to Bar product(s) containing Chardonnay marc on cardiometabolic health. These initial studies will inform the design and timing of data collection for future dietary intervention trials that will examine the influence of Chardonnay marc intake on outcomes/biomarkers of both cardiometabolic health and the gut microbiome. This includes collecting data on the potential differences in response to the products based on the unique food matrix for each of the products that will be tested. Moreover, as there is a paucity of data on the influence of cocoa flavanol intake on vascular function beyond 4 hours post intake, the response of the selected outcomes will be assessed after 6 hours of flavanol intake. This is a time point that captures the increased circulating presence of microbial derived flavanol metabolites.

Sponsor: University of California, Davis

Who Can Participate

Inclusion Criteria

Screening or Visit 1 Reactive Hyperemia Index (RHI; EndoPAT 2000) \< 2.0
Subject is willing and able to comply with the study protocols.
Subject is willing to participate in all study procedures
BMI 25.0 - 35 kg/m2

Exclusion Criteria

BMI ≥ 35 kg/m2
Indivduals that weight less than a 110 lbs
Donation of blood within the previous 30 days
Visit 1 Reactive Hyperemia Index (RHI; EndoPAT 2000) ≥ 2.0
1 ug/ml and 3 ug/ml collagen screening maximal platelet aggregatory response of \< 65%.
Platelet counts \< 150,000 / ul
Anemia, which includes self report, or a screening hemoglobin and hematocrit that is less than the normal reference range or as diagnosed by study physician upon review of complete blood cell count reports.
Dislike or allergy for nuts, cocoa or grape products
Self-reported use of daily anticoagulation agents including aspirin, NSAIDs
Vegan, Vegetarians, food faddists or those consuming a non-traditional diet
Fruit consumption ≥ 3 cups/day
Vegetable consumption ≥ 4 cups/day
Nut intake ≥ 2 servings/ week
Coffee/tea ≥ 3 cups/day
Dark chocolate ≥ 3 oz/day
Self-reported restriction of physical activity due to a chronic health condition
Self-reported chronic/routine high intensity exercise
Self-reported diabetes
Blood pressure ≥ 140/90 mm Hg
Self-reported renal or liver disease
Self-reported heart disease, which includes cardiovascular events and stroke
Peripheral artery disease, Raynaud's syndrome
Inability to properly place or wear the PAT probes or abnormal measurements on pre- screening PAT
Self-reported cancer within past 5 years
Self-reported malabsorption
Currently taking prescription drugs or supplements.
Supplement use or unwillingness to stop any supplement use, including herbal, plant or botanical, fish oil, oil supplements a month prior to study enrollment.
Indications of substance or alcohol abuse within the last 3 years
smoking, vaping, cannabis use
Current enrollee in a clinical research study.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Davis?

Yes, this clinical trial (NCT05545865) has an active research site in Davis, CA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Cardiovascular Diseases Treatment Options in Davis, CA

If you're searching for cardiovascular diseases treatment options in Davis, CA, this clinical trial (NCT05545865) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Davis research site is actively enrolling participants for this clinical trial. You'll receive care from experienced cardiovascular diseases specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all cardiovascular diseases clinical trials near you to find additional studies recruiting in your area.

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