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Comparison of Acute Tart Cherry Supplement Formulation and Dose on Inflammation and Oxidative Capacity

Comparison of Acute Tart Cherry Supplement Formulation and Dose on Inflammation and Oxidative Capacity

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04497077
Enrollment
48
Registered
2020-08-04
Start date
2015-09-15
Completion date
2017-05-30
Last updated
2020-08-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inflammation, Oxidative Stress

Brief summary

A comparison of acute tart cherry formations (juice vs. powdered) and doses (single vs. twice daily) on inflammation and oxidative capacity.

Detailed description

Participants will be randomly allocated to a group: one tart cherry capsule daily, two tart cherry capsules daily, one 8oz. bottle of tart cherry juice daily, two 8oz. bottles of tart cherry juice taken 8 hours apart, one placebo pill, and one 8oz. bottle of placebo. Participants will arrive to the lab at 8 am after an overnight fast of 10 hours. They will provide a blood sample and then ingest their study treatment. Participants will stay in the lab for a further 2 hours for additional blood draws then return to the lab in 6 hours for another blood draw. At this time if they are in a twice daily group they will receive their second treatment for the day. All participants will come back to the lab 24 hours later where they will give a blood sample and receive their next treatment. If they are in the twice daily group they will be provided with their next dose and given instructions to consume it in 8 hours. Participants will arrive 24 hours later for a final blood draw with no supplementation. Blood samples will be measured pre-ingestion, 1 hour, 2 hours, 8 hours, 24 hours and 48 hours post-ingestion. Samples will be analyzed for plasma oxygen radical absorbance capacity (ORAC), uric acid (UA), and C-reactive protein (CRP).

Interventions

DIETARY_SUPPLEMENTtart cherry

Either tart cherry juice or freeze dried powdered tart cherry in capsule was given

DIETARY_SUPPLEMENTplacebo

either cornstarch capsule or kool-aid

Sponsors

Marywood University
CollaboratorOTHER
Ohio University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* free of cardiovascular, metabolic and inflammatory conditions * non-smokers * no known allergy to cherries or cherry juice * not be taking food supplements (turmeric/curcumin, cherry products, greens, etc.).

Exclusion criteria

* quit smoking less than one year ago. * currently being treated for arthritis or an inflammatory condition. * currently being treated for uncontrolled cardiovascular disease, high blood pressure, diabetes, fibromyalgia, or irritable bowel syndrome. * pregnant. * regularly consume cherries or are allergic to cherries or dairy. * currently use anti-inflammatory medications, * have used corticosteroids in the last two months.

Design outcomes

Primary

MeasureTime frameDescription
Change in c-reactive protein1 hour, 2 hours, 8 hours, 24 hours, and 48 hours post ingestionc-reactive protein (mg/L) measured via assay
Change in uric acid1 hour, 2 hours, 8 hours, 24 hours, and 48 hours post ingestionuric acid (mg/dL) measured via assay
Change in oxidative capacity1 hour, 2 hours, 8 hours, 24 hours, and 48 hours post ingestionoxygen radical absorbance capacity (uM Trolox equivalents) measured via assay

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026