Effects of Supplementation in Healthy Russian Population
NCT ID: NCT02224092
Last Updated: 2014-08-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
120 participants
INTERVENTIONAL
2010-10-31
2013-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
DOUBLE
Study Groups
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Active
Active is a multivitamin multimineral with phytonutrient product.
multivitamin multimineral with phytonutrient supplementation
The multivitamin multimineral with phytonutrient product consists of four tablets per dose, two "Vitamin" tablets, a "Mineral" tablet, and a "Phytonutrient" tablet. The placebo for this trial will be formulated to match the shape and color of all multivitamin multimineral with phytonutrient product tablets, e.g., a Vitamin Placebo, a Mineral Placebo and a Phytonutrient Placebo.
Placebo
Placebo is a sugar pill.
multivitamin multimineral with phytonutrient supplementation
The multivitamin multimineral with phytonutrient product consists of four tablets per dose, two "Vitamin" tablets, a "Mineral" tablet, and a "Phytonutrient" tablet. The placebo for this trial will be formulated to match the shape and color of all multivitamin multimineral with phytonutrient product tablets, e.g., a Vitamin Placebo, a Mineral Placebo and a Phytonutrient Placebo.
Interventions
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multivitamin multimineral with phytonutrient supplementation
The multivitamin multimineral with phytonutrient product consists of four tablets per dose, two "Vitamin" tablets, a "Mineral" tablet, and a "Phytonutrient" tablet. The placebo for this trial will be formulated to match the shape and color of all multivitamin multimineral with phytonutrient product tablets, e.g., a Vitamin Placebo, a Mineral Placebo and a Phytonutrient Placebo.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Individual should be judged to be in good general health on the basis of an interview and abbreviated physical exam.
* Individual understands the procedures and agrees to participate in the study.
* Individual is able and willing to provide written informed consent and confidentiality agreement.
Exclusion Criteria
* Presence of cardiovascular disease, hypercholesterolemia, cancer, diabetes mellitus, or any other chronic health condition identified from the findings of the interview.
* Currently treated for uncontrolled hypertension or blood pressure greater \> 140 mm Hg systolic or \> 90 mm Hg diastolic during seated, resting measurement on two consecutive occasions during visit 1.
* Therapeutic uses of coumadin, aspirin, or other medications that influence hemostasis within four weeks of Day 1.
* Participation in another clinical trial within 30 days of enrollment into the study.
* History or current abuse of drugs or alcohol, or intake \> 4 alcoholic beverages per day.
* Known hypersensitivity to study product or any ingredient in study product.
* A change in hormone therapy, including oral contraceptives, within 4 weeks prior to screening, or unwilling to maintain current hormone therapy/oral contraceptive use throughout the course of the study.
* Pregnant or lactating women, or women of child-bearing potential unwilling to use a medically approved form of birth control.
* Any condition that the Principal Investigator believes may put the subject at undue risk.
40 Years
70 Years
ALL
Yes
Sponsors
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Russian Institute of Nutrition
UNKNOWN
Access Business Group
INDUSTRY
Responsible Party
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Principal Investigators
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Vasily A Isakov, M.D., Ph.D.
Role: PRINCIPAL_INVESTIGATOR
Russian Institute of Nutrition
Locations
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Russian Institute of Nutrition
Moscow, , Russia
Countries
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Other Identifiers
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Amway-2010-RU1
Identifier Type: -
Identifier Source: org_study_id
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