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Effects of LopiGLIK® on Cardiovascular Risk

Effects of a New Combination of Nutraceutics (LopiGLIK®) on Cardiovascular Risk

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02898805
Acronym
LopiWEB
Enrollment
600
Registered
2016-09-13
Start date
2016-01-31
Completion date
2018-12-01
Last updated
2019-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Risk Factors

Brief summary

The study is designed to compare the effects of two combination of nutraceuticals: Armolipid Plus® and LopiGLIK® (Akademy Pharma), a new supplement that, in addition to Berberine and Red Rice, contains Morus Alba's extract. The study will analyze the impact of 16 week treatment with one of the combinations, according to a randomized scheme, on metabolic parameters in dyslipidemic subjects that do not require or not tolerate a statin therapy. In particular, it will assess the ability of the two combinations to reduce the levels of total and LDL cholesterol, HbA1C, glicaemia and insulin and increase those of HDL cholesterol.

Detailed description

The experimental design involves the construction of a multi-center, controlled, randomized, single-blind, versus Armolipid Plus®. Patients with mild hypercholesterolemia, of both sexes and aged between 18 and 75 years, will be recruited, from the beginning of the study and for the next 2 weeks, from 30 Cv specialists and/or GPs (25 patients each). The subjects will be enrolled in the 50/50% male/female ratio ± 10% comparable for age, in order to obtain a proper comparison between groups with similar demographic characteristics or not statistically different. The subjects, selected on the basis of inclusion and exclusion criteria, will be divided into two groups, subjected to centralized randomization at the Diagnosis and Treatment of hypertension Center to receive one of two different treatments, a tablet/day of the new nutraceutical LopiGLIK® (Akademy Pharma) containing Morus Alba, immediately after a meal, vs. a tablet/day of Armolipid Plus, always immediately after the meal. During the first two weeks both groups will follow the prescribed diet and assume the placebo. At the end, blood tests (traditional metabolic parameters, blood glucose, HbA1C, fasting insulin, transaminase levels, CPK) and the endothelial function will be assesed. During the next 16 weeks a group will assume LopiGLIK® (Akademy Pharma) containing Morus Alba, the other will assume Armolipid Plus and everyone will continue to follow the prescribed diet. At the end of this period blood tests will be repeated. Tablets of Armolipid Plus, LopiGLIK® and placebo will be provided by Akademy Pharma free of charge

Interventions

OTHERPlacebo
OTHERPrescribed Diet
DIETARY_SUPPLEMENTLopiGLIK®
DIETARY_SUPPLEMENTArmolipid Plus

Sponsors

Federico II University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Total Cholesterol\<300 mg/dL * Total Cholesterol\>200 mg/dL * Cardiovascular Risk\<20%

Exclusion criteria

* Pregnancy * Documented intolerance to one or more 'components LOPIGLIK / Armolipid PLUS * Previous cardiovascular events * Familiar severe dyslipidemia * Familiar high cardiovascular risk Hepatic or muscular disorders Subjects receiving lipid-lowering drugs

Design outcomes

Primary

MeasureTime frame
Reduction of LDL-Cholesterol levels16 weeks

Secondary

MeasureTime frame
Increasing of HDL-Cholesterol levels16 weeks
Reduction of HbA1c levels16 weeks
Reduction of fastin insuline levels16 weeks

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026