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Completed

NCT Number: NCT07142720

Rapid Effects on Antioxidant Status, Immune Alertness, and Regenerative Activity

This clinical study aims at documenting rapid effects after consuming single doses of test product, when compared to consuming a placebo.

A double-blind, placebo-controlled, cross-over study design will be used.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

NIS Labs

Klamath Falls, Oregon, 97601, United States

About this study

For each participant, the clinic visits are scheduled at the same time of the day during the morning hours of 7-11 am to control for the effect of circadian fluctuations. One clinic visit involves consuming a placebo and serves as a control for the circadian variations in cytokine levels and immune surveillance for each participant. Since there is interference from exercise and stress with the release versus homing of lymphocytes, the study environment is managed so that any physical and mental stress is minimized during each visit. Upon arrival at a clinic visit, participants complete a questionnaire to help monitor exceptional circumstances that may influence the stress level of that person on that day. Predetermined criteria for re-scheduling a visit include sleep deprivation and acute anxiety. After completing the questionnaire, participants are instructed to remain calm and inactive for 3 hours, comfortably seated in a chair. After the first hour, the baseline blood sample is drawn. Immediately after the baseline sample is drawn, a test product is provided and consumed in the presence of clinic staff. Blood samples are drawn at 1 hour and 2 hours after consumption of the test product or placebo.

The blood is tested for antioxidant status, immune cell surveillance, and regenerating properties involving stem cell surveillance. The process of surveillance is the natural process of our immune and stem cells to move through our body and detect problems that need repair. In addition, blood samples are tested for changes to pro- and anti-inflammatory cytokines, antiviral peptides, and restorative growth factors.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Healthy adults;
  • Age 18-75 years (inclusive);
  • Veins easy to see in one or both arms (to allow for the multiple blood draws);
  • Willing to comply with a 24-hour wash-out period for vitamins and nutritional supplements;
  • Willing to comply with study procedures, including:
  • Maintaining a consistent diet and lifestyle routine throughout the study,
  • Consistent habit of bland breakfasts on days of clinic visits,
  • Abstaining from exercising and nutritional supplements on the morning of a study visit,
  • Abstaining from use of coffee, tea, and soft drinks for at least one hour prior to a clinic visit;
  • Abstaining from music, candy, gum, computer/cell phone use, during clinic visits.

Exclusion criteria

  • Previous major gastrointestinal surgery (absorption of test product may be altered) (minor surgery not a problem, including previous removal of appendix and gall bladder);
  • Taking anti-inflammatory medications on a daily basis;
  • Currently experiencing intense stressful events/life changes;
  • Currently in intensive athletic training (such as marathon runners);
  • Currently taking antipsychotic medications such as clozapine, Risperdal, Abilify, Zyprexa or Seroquel;
  • An unusual sleep routine (examples: working graveyard shift, irregular routine with frequent late nights, studying, partying);
  • Unwilling to maintain a constant intake of supplements over the duration of the study;
  • Anxiety about having blood drawn;
  • Women of childbearing potential: Pregnant, nursing, or trying to become pregnant;
  • Known food allergies related to ingredients in active test product or placebo.

Treatment and study plan

A low dose of seaweed extract

Dietary Supplement

A low dose of the seaweed extract is dissolved in plain rice milk to help camouflage the strong algae-taste.

A high dose of seaweed extract

Dietary Supplement

A high dose of the seaweed extract is dissolved in plain rice milk to help camouflage the strong algae-taste.

Placebo

Dietary Supplement

Plain rice milk.

Primary outcomes

  1. Antioxidant uptake and protection

    Time frame: 1 and 2 hours

    Changes to antioxidant status of blood samples

Secondary outcomes

  1. Immune cell numbers in blood

    Time frame: 1 and 2 hours

    Changes to immune cell trafficking and status of immune cell alertness, ie. the changes in immune cell populations and activation following consumption: Numbers of CD3- CD56+ NK cells in blood Numbers of CD3+ CD56+ NKT cells in blood Numbers of CD3+ CD56- T cells in blood Numbers of cells positive for CD25 Numbers of cells positive for CD69

Other outcomes

  1. Stem Cell Numbers in Blood

    Time frame: 1 and 2 hours

    Changes to stem cell surveillance, i.e. the changes in stem cell populations following consumption of the study product: Numbers of CD45dimCD34+CD309+ pluripotential stem cells Numbers of Cd45dim CD34+CD309- progenitor stem cells Numbers of CD45-CD90+ lymphocytes in blood Numbers of CD31++ CD34- endothelial stem cells in blood

  2. Communication through cytokines.

    Time frame: 1 and 2 hours

    Serum levels of cytokines, antiviral peptides, and restorative growth factors.

Sponsors and collaborators

Lead sponsor

Natural Immune Systems Inc

Other

Registry information

Official study title

Clinical Study on Rapid Effects on Antioxidant Status, Immune Alertness, and Regenerative Activity

Important dates

Study start
2022
Primary completion
2024
Study completion
2025
First posted
Aug 27, 2025
Registry last updated
Jan 30, 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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