Clinical Study on Rapid Antioxidant Protection and Immune Modulating Effects.
Not Applicable
- Conditions
- Pharmacokinetics
- Registration Number
- NCT05042674
- Lead Sponsor
- Natural Immune Systems Inc
- Brief Summary
A trial on acute antioxidant protection and immune effects when 24 people consume a novel nutraceutical blend compared to a placebo on different test days.
- Detailed Description
A randomized, cross-over study design will be used to evaluate immune effects of consumption of 25 mg ergothioneine. On the first clinic day, participants will take a placebo with a one week wash out. Following the wash out week, participants will take 25 mg ergothioneine for 7 consecutive days.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 24
Inclusion Criteria
- Willing to comply with a 24-hour wash-out period for vitamins and nutritional supplements
- Willing to maintain a consistent diet and lifestyle routine throughout the study
- Willing to avoid consumption of meals where the predominant ingredients include mushrooms, seafood, and organ meat (liver, heart).*
- Willing to abstaining from exercising on the morning of a study visit
- Willing to abstain from use of coffee, tea, and soft drinks for at least one hour prior to a clinic visit
- Willing to abstain from music, candy, gum, computer/cell phone use, during clinic visits.
Exclusion Criteria
- Previous major gastrointestinal surgery
- Active chronic immunological disease
- Currently taking daily OTC medications, prescription pain medications, antipsychotic medications, anti-inflammatory nutritional supplements judged by the study coordinator to negate or camouflage the effects if the test product, nutritional supplements containing medicinal mushroom extracts
- Diagnose with Type I diabetes, autoimmune disorders
- Getting regular joint injections
- Active severe chronic disease (such as HIV, chronic hepatitis)
- Currently experiencing intense stressful events/ life changes
- Currently in intensive athletic training
- Experiencing an unusual sleep routine
- Unwilling to maintain a constant intake of supplements over the duration of the study
- Anxiety about having blood drawn
- Women who are pregnant, nursing, or trying to become pregnant
- Known food allergies to ingredients in test product
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Change in level of reduced glutathione 2 hours Mean fluorescence
- Secondary Outcome Measures
Name Time Method Change in mitochondrial mass and mitochondrial potential from baseline 2 hours Mean fluorescence
Trial Locations
- Locations (1)
NIS Labs
🇺🇸Klamath Falls, Oregon, United States
NIS Labs🇺🇸Klamath Falls, Oregon, United StatesGitte Jensen, PhDContact541-884-0112gitte@nislabs.comGitte S Jensen, PhDPrincipal Investigator