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You can access this
if you have
and you are
between 18 and 75
This is a second phase trial assessing
efficacy and side effects of the new treatment.
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The overall objective of the study is to assess the efficacy of Coleosoma formulation (fermented red rice, berberine and chitosan) in reducing non-HDL cholesterol in dyslipidemic patients.
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Locations near you
Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Full eligibility criteria for NCT03027336
Ages eligible for Study
18 Years to 75 Years
Genders eligible for Study
Accepts Healthy Volunteers
non-HDL cholesterol ≥ 160 mg/dl;
providing their written Informed Consent;
capable of understanding the nature, purpose and study procedures
diabetes (ADA criteria)
reduced renal (GFR<60 mL/min/1.73m2) or hepatic (transaminase levels >2.5 folds the upper reference limit) function;
present or past history of alcohol or drug abuse
cerebro-vascular and neoplastic diseases in the 5 years prior to study visit
use of drugs or food supplements interfering with cholesterol levels
pregnancy or breastfeeding;
participation in other clinical trials in the previous 30 days;
All locations for NCT03027336
Parma, Italy, 43126
View full eligibility
Tris trial is registered with FDA with number:
. The sponsor of the trial is
Azienda Ospedaliero-Universitaria di Parma
and it is
looking for 39 volunteers
for the current phase.
Official trial title:
Randomized Controlled Clinical Trial for Assessing Tolerability and Effectiveness of Formula Coleosoma 29 in Patients With Dyslipidemia
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