LIFEHOUSE: Description of the Tent Bucket -Immune Support
Sponsored by Metagenics, Inc.
About this trial
Last updated 3 years ago
Study ID
Status
Type
Phase
Placebo
Accepting
Trial Timing
Ended 2 years ago
What is this trial about?
What are the participation requirements?
Inclusion Criteria
- Male or Female
- Ages 18-69, inclusive
- Metagenics' employees in Gig Harbor, WA; Colonial Heights, VA; Lenexa, KS, and Santa Fe Springs, CA
- General good health
- Willing to give written informed consent to participate in the study
Exclusion Criteria
- An allergy to any ingredient in Vit.D3 5000 and/or Immune Active
- A serious, unstable illness including cardiac, hepatic, renal, gastrointestinal, respiratory, endocrinologic, neurologic, psychiatric, immunologic/rheumatological, or oncological/hematologic disease.
- Hyperparathyroidism
- Granulomatous disorders including as sarcoidosis, tuberculosis, leprosy, berylliosis, histoplasmosis, and coccidioidomycosis
- Chronic renal insufficiency
- Nephrolithiasis
- Prior cancer diagnosis
- Known infection with human immunodeficiency virus (HIV), tuberculosis (TB), or Hepatitis B or C.
- Established psychiatric disease including moderate to severe depression, thought disorders and bipolar disorder
- Planned use of nutritional supplements (exclusive of multiple vitamin/mineral supplements and medical foods) containing in total more than 1,000 IU Vitamin D3 and/or 10 mg Zinc
- Use of pharmaceutical nitrates for any indication
- Use of drugs of abuse and recreational drugs/substances (such as but not limited to opioids, cocaine, phencyclidine (PCP), and methamphetamine)
- History of marijuana or cannabinoid abuse within 12 months prior to screening and for the duration of the study.
- History of alcohol abuse or a diagnosis of alcoholism within 12 months prior to screening and for the duration of the study.
- Pregnant or breastfeeding women
- Inability to comply with study and/or follow-up visits.
- Any concurrent condition (including clinically significant abnormalities in medical history, physical examination or laboratory evaluations) which, in the opinion of the Principal Investigator (PI), would preclude safe participation in this study or interfere with compliance.
- Any sound medical, psychiatric, and/or social reason which, in the opinion of the PI, would preclude safe participation in this study or interfere with compliance.