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Completed

NCT Number: NCT06944210

Evaluation of the Antioxidant and Anti-Inflammatory Capacities of the 'Rosy Red Valencia' and 'Olinda Valencia' Sweet Orange Varieties in Healthy Subjects

This study aims to evaluate the antioxidant and anti-inflammatory effects of acute and chronic consumption of two sweet orange (Citrus sinensis) varieties-'Rosy Red Valencia', which is rich in carotenoids such as lycopene, phytoene, and phytofluene, and 'Olinda Valencia', which lacks these carotenoids-in healthy adults. In this 4-week, randomized, parallel-arm clinical trial, participants will consume either 'Rosy Red Valencia' or 'Olinda Valencia' oranges daily. The study will assess the effects of sweet orange intake on markers of oxidative stress and inflammation, plasma carotenoid concentrations, gene expression in peripheral blood mononuclear cells, and gut health. Findings from this study may help identify potential health benefits associated with specific carotenoid profiles in sweet oranges and provide insights into their role in modulating inflammation and oxidative stress.

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Key information

Age range

25 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Nutrition Department, Ragle Facility, University of California Davis

Davis, California, 95616, United States

About this study

The health benefits of orange consumption have been described; however, the specific bioactive compounds responsible for these effects, as well as the underlying mechanisms of action, are not fully understood. There are several varieties of sweet oranges, each with a unique phytochemical profile and potentially distinct health-promoting properties. The 'Rosy Red Valencia' sweet orange is enriched in carotenoids such as lycopene, phytoene, and phytofluene, whereas the commonly consumed 'Olinda Valencia' contains negligible levels of these compounds.

This randomized, parallel-arm clinical trial aims to evaluate and compare the antioxidant and anti-inflammatory effects of 'Rosy Red Valencia' and 'Olinda Valencia' sweet orange consumption in healthy men and women. Participants will be randomized to consume one of the two orange varieties twice daily for four weeks.

The study includes both an acute phase (1-day consumption) and a chronic phase (4-week daily consumption). Blood samples will be collected at baseline, after 1 day, and after 4 weeks of consumption to assess changes in plasma carotenoid concentrations, markers of oxidative stress and inflammation, and gene expression profiles in peripheral blood mononuclear cells. Fecal samples will be collected at baseline and after 4 weeks to assess the effects on gut microbiota composition. By evaluating and comparing the biological effects of these two orange varieties, the study aims to elucidate the role of specific carotenoids in mediating the health benefits of sweet orange consumption.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy men and women
  • Age Range: 25-40 years
  • Body mass index (BMI) with values between 21 and 29.9 kg^m2
  • Willingness to accept randomization, undergo the testing and intervention procedures, and deliver blood and stool samples
  • Willingness to refrain from consuming foods rich in lycopene, phytoene, and phytofluene and limit the intake of some polyphenol-rich foods
  • Willingness to discontinue the use of antioxidant supplements (such as carotenoid, polyphenol supplements), prebiotics and/or probiotics

Exclusion criteria

  • Pregnancy/lactation
  • History of cardiovascular diseases, diabetes, uncontrolled hypertension, heart failure, stroke, liver, gallbladder, kidney, thyroid disease, gastrointestinal, autoimmune disorder, or cancer.
  • Psychiatric disease that interferes with the understanding and implementation of the intervention
  • History of eating disorders (such as bulimia nervosa and anorexia nervosa) in the last 5 years
  • Current smokers
  • Vegan, vegetarian, or other special diets (e.g., keto, paleo)
  • Use of antibiotics or laxatives in the previous month
  • History of substance abuse or alcohol abuse
  • involvement in a weight loss intervention program within the past month or weight change > 10%
  • Self-report of allergic reactions to study products or their phytochemicals.

Treatment and study plan

'Rosy Red Valencia' sweet orange

Other

The participants consume 2 'Rosy Red Valencia' sweet oranges daily for 4 weeks

'Olinda Valencia' sweet oranges

Other

The participants consume 2 'Olinda Valencia' sweet oranges daily for 4 weeks

Primary outcomes

  1. Levels of lycopene and noncolored carotenoids

    Time frame: 0, 1 day, 4 weeks

    Levels in plasma

Secondary outcomes

  1. Oxidative stress

    Time frame: 0, 1 day, 4 weeks

    Oxidative stress marker DNA/RNA oxidative damage assessed in blood samples from participants by a commercial kit

  2. Inflammation

    Time frame: 0, 1 day, 4 weeks

    Levels of inflammatory marker CRP assessed in blood samples from participants using commercial assay kits.

  3. Gene expression

    Time frame: 0, 1 day, 4 weeks

    Gene expression in Peripheral Blood Mononuclear Cells (PBMCs)

  4. Microbiota composition

    Time frame: 0, 4 weeks

    From stool samples

  5. Lipid/metabolic profile

    Time frame: 0, 4 weeks

    Measured in blood samples

  6. Systolic and diastolic blood pressure

    Time frame: 0, 4 weeks

    Measured by automated sphygmomanometer

Sponsors and collaborators

Lead sponsor

University of California, Davis

Other

Registry information

Important dates

Study start
2025
Primary completion
2025
Study completion
2026
First posted
Apr 25, 2025
Registry last updated
Mar 11, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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