Effect Of Capros Supplementation On Cardiovascular Disease Risk Factors In Humans
Completed · Not applicable
Conditions studied: Hyperlipidemia
In brief
The hypothesis of this study is that the natural supplement Capros will decrease LDL levels, platelet aggregation, and serum concentrations of high sensitivity C-reactive protein in humans at risk for cardiovascular disease.
Key facts
- Study ID
- NCT01858376
- Run by
- Chandan K Sen
- People needed
- 24
- Starts
- 2013-03-01
- Expected to finish
- 2015-01-01
- Last updated by the study team
- 2018-07-27
Who can join
Age: 21 and older, up to 70. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Patients 21-70 years of age
- BMI 25-35
You may not qualify if…
- BMI > 35 OR < 25
- Smokers
- Individuals who are deemed unable to understand the procedures, risks and benefits of the study, i.e. Informed consent will be excluded
- Females who are pregnant as well as individuals who are therapeutically immuno-compromised will also be excluded in order to minimize the risk to such individuals (and fetus) and to decrease statistical variability and to minimize potential of confounders.
- Candidates for inclusion into the study will not include individuals as defined in 45 CFR 46 Subparts B, C and D, nor from any other population which may be considered vulnerable. Pregnant women are excluded to minimize the risk to such individuals (and fetus) and to decrease statistical variability and to minimize potential of confounders.
Where it is running
- The Ohio State University — Columbus, Ohio, United States
Full record on ClinicalTrials.gov
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