Efficacy and Tolerability of the Nutraceutical Formulation Coleosoma in Dyslipidemic Subjects (Coleosoma)
Primary Purpose
Dyslipidemias
Status
Completed
Phase
Phase 2
Locations
Italy
Study Type
Interventional
Intervention
Coleosoma
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Dyslipidemias focused on measuring dyslipidemia, dietary supplement
Eligibility Criteria
Inclusion Criteria:
- non-HDL cholesterol ≥ 160 mg/dl;
- providing their written Informed Consent;
- capable of understanding the nature, purpose and study procedures
Exclusion Criteria:
- 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;
- monogenic dyslipidemia;
- participation in other clinical trials in the previous 30 days;
- uncompensated hypothyroidism
Sites / Locations
- Endocrinology Unit
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
coleosoma
placebo
Arm Description
coleosoma 500mg tablet daily
placebo tablets
Outcomes
Primary Outcome Measures
Change from baseline values of non-HDL cholesterol (mg/dl) after 12 weeks of coleosoma treatment vs placebo
Difference in the non-HDL cholesterol value compared to baseline in the 2 arms.
Secondary Outcome Measures
change from baseline values of non-HDL cholesterol (mg/dl) at 4 weeks of coleosoma treatment vs placebo
Difference in the non-HDL cholesterol value compared to baseline in the 2 arms.
change from baseline values of Free Plasma Glucose (mg/dl) at 12 weeks of coleosoma treatment vs placebo
Difference in the Free Plasma Glucose value compared to baseline in the 2 arms.
change from baseline values of Body Mass Index (Kg/m2) at 12 weeks of coleosoma treatment vs placebo
Difference in the BMI value compared to baseline in the 2 arms.
change from baseline values of waist circumference (cm) at 12 weeks of coleosoma treatment vs placebo
Difference in the waist circumference value compared to baseline in the 2 arms.
Change from baseline values of HbA1C (%) at 12 weeks of coleosoma treatment vs placebo
Difference in the HbA1C value compared to baseline in the 2 arms.
Change from baseline values of LDL Cholesterol, triglycerides and HDL cholesterol at 12 weeks of coleosoma treatment vs placebo
Difference in theLDL Cholesterol, triglycerides and HDL cholesterol value compared to baseline in the 2 arms.
All these parameters have the same Units of Measure (mg/dl)
Change from baseline values of ApoB/Apo A1 ratio at 12 weeks of coleosoma treatment vs placebo
Difference in the ApoB/Apo A1ratio compared to baseline in the 2 arms.
Change from baseline values of inflammatory cytokines (IL-1, IL6, IL-10, hsPCR, TNFalpha ) at 12 weeks of coleosoma treatment vs placebo
Difference in the inflammatory cytokines value compared to baseline in the 2 arms.
All these parameters have the same Units of Measure (pg/ml)
Change from baseline values of insulin (pmol/l) at 12 weeks of coleosoma treatment vs placebo
Difference in the insulin value compared to baseline in the 2 arms.
Change from baseline values of hormone profile (glucagon, active GLP-1 and GIP) at 12 weeks of coleosoma treatment vs placebo
Difference in the hormone profile compared to baseline in the 2 arms. All these parameters have the same Units of Measure (pg/ml)
Change from baseline values of Endothelial Progenitor Cells (EPC) number at 12 weeks of coleosoma treatment vs placebo
Difference in the EPC number compared to baseline in the 2 arms.
Full Information
NCT ID
NCT03027336
First Posted
January 12, 2017
Last Updated
January 19, 2017
Sponsor
Azienda Ospedaliero-Universitaria di Parma
Collaborators
DOC generici srl
1. Study Identification
Unique Protocol Identification Number
NCT03027336
Brief Title
Efficacy and Tolerability of the Nutraceutical Formulation Coleosoma in Dyslipidemic Subjects
Acronym
Coleosoma
Official Title
Randomized Controlled Clinical Trial for Assessing Tolerability and Effectiveness of Formula Coleosoma 29 in Patients With Dyslipidemia
Study Type
Interventional
2. Study Status
Record Verification Date
January 2017
Overall Recruitment Status
Completed
Study Start Date
January 2016 (undefined)
Primary Completion Date
August 2016 (Actual)
Study Completion Date
October 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Azienda Ospedaliero-Universitaria di Parma
Collaborators
DOC generici srl
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
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.
Detailed Description
The incidence of cardiovascular diseases related to atherosclerosis is the leading cause of death in industrialized countries and in many developing countries. It becomes, therefore, essential to implement preventive strategies with lifestyle changes in order to prevent / control the risk factors related to cardiovascular disease.
Dyslipidemia is characterized by qualitative and quantitative alterations of plasma lipids and lipoproteins. In subjects where it is not yet indicated a statin therapy, the guidelines recommend a lifestyle (diet and exercise) act to control cardiovascular risk factors.
The formulation Coleosoma is a supplement composed of fermented red rice, berberine and chitosan. Aim of the study is to evaluate the effectiveness of coleosoma formulation in reducing non-HDL cholesterol (Non-HDL-C), which provides a measure of the cholesterol content in all atherogenic particles.
This is a single-center, randomized (3:1) and controlled double-blind phase II study that involve dyslipidemic patients with non-HDL cholesterol levels ≥ 160 mg / dl.
The study included a maximum of 4 visits for all subjects enrolled. All eligible patients at V0 (screening) undergo baseline assessments (V1) and have been allocated according to the procedure of randomization to one of the study arms. Follow-up (FU) visits for all subjects was at 4 (V2) and at 12 weeks (V3) after randomization.
Laboratory and diagnostic:
At each visits patients undergo: anthropometric and hemodynamic assessment: weight and height for Body Mass Index (BMI) calculation, waist circumference, blood pressure, heart rate; blood collection for metabolic/hormonal profile: fasting plasma glucose, HbA1c, insulin, glucagon, active glucagon-like peptide-1 (GLP-1), total gastric inhibitory polypeptide (GIP), total cholesterol, HDL-cholesterol, triglycerides, aspartate aminotransferase (AST), alanine aminotransferase (ALT), creatinine, creatine phosphokinase (CPK), apolipoprotein (Apo) B, Apo A1, and inflammatory cytokines (IL-1, IL-6, IL-10, high-sensitivity C Reactive Protein (hsPCR), TNFalpha).
At V1 and V2 the Endothelial Progenitor Cells (EPC) number was evaluated with a cytofluorimetric assay.
Safety analysis has been conducted after 12 weeks treatment by determining ALT, CPK and estimated Glomerular filtration rate (eGFR) values.
This study has been sponsored by DOC generici s.r.l.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dyslipidemias
Keywords
dyslipidemia, dietary supplement
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
The study included two arms: a treatment arm with dietary supplement (Coleosoma) and a placebo arm.
Coleosoma is the name of a new patented dietary supplement composed by Berberin 200 mg, Fermented Red Rice from Monascus purpureus 100 mg (correspondiing at 3 mg of monacolin K), Chitosan 100 mg e Q10 Coenzyme10 mg
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
39 (Actual)
8. Arms, Groups, and Interventions
Arm Title
coleosoma
Arm Type
Experimental
Arm Description
coleosoma 500mg tablet daily
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
placebo tablets
Intervention Type
Dietary Supplement
Intervention Name(s)
Coleosoma
Other Intervention Name(s)
TegraDOC
Intervention Description
patients will take one tablet of 500mg daily for 12 weeks. No dose titration is foreseen.
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
patients will take one tablet daily for 12 weeks.
Primary Outcome Measure Information:
Title
Change from baseline values of non-HDL cholesterol (mg/dl) after 12 weeks of coleosoma treatment vs placebo
Description
Difference in the non-HDL cholesterol value compared to baseline in the 2 arms.
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
change from baseline values of non-HDL cholesterol (mg/dl) at 4 weeks of coleosoma treatment vs placebo
Description
Difference in the non-HDL cholesterol value compared to baseline in the 2 arms.
Time Frame
4 weeks
Title
change from baseline values of Free Plasma Glucose (mg/dl) at 12 weeks of coleosoma treatment vs placebo
Description
Difference in the Free Plasma Glucose value compared to baseline in the 2 arms.
Time Frame
12 weeks
Title
change from baseline values of Body Mass Index (Kg/m2) at 12 weeks of coleosoma treatment vs placebo
Description
Difference in the BMI value compared to baseline in the 2 arms.
Time Frame
12 weeks
Title
change from baseline values of waist circumference (cm) at 12 weeks of coleosoma treatment vs placebo
Description
Difference in the waist circumference value compared to baseline in the 2 arms.
Time Frame
12 weeks
Title
Change from baseline values of HbA1C (%) at 12 weeks of coleosoma treatment vs placebo
Description
Difference in the HbA1C value compared to baseline in the 2 arms.
Time Frame
12 weeks
Title
Change from baseline values of LDL Cholesterol, triglycerides and HDL cholesterol at 12 weeks of coleosoma treatment vs placebo
Description
Difference in theLDL Cholesterol, triglycerides and HDL cholesterol value compared to baseline in the 2 arms.
All these parameters have the same Units of Measure (mg/dl)
Time Frame
12 weeks
Title
Change from baseline values of ApoB/Apo A1 ratio at 12 weeks of coleosoma treatment vs placebo
Description
Difference in the ApoB/Apo A1ratio compared to baseline in the 2 arms.
Time Frame
12 weeks
Title
Change from baseline values of inflammatory cytokines (IL-1, IL6, IL-10, hsPCR, TNFalpha ) at 12 weeks of coleosoma treatment vs placebo
Description
Difference in the inflammatory cytokines value compared to baseline in the 2 arms.
All these parameters have the same Units of Measure (pg/ml)
Time Frame
12 weeks
Title
Change from baseline values of insulin (pmol/l) at 12 weeks of coleosoma treatment vs placebo
Description
Difference in the insulin value compared to baseline in the 2 arms.
Time Frame
12 weeks
Title
Change from baseline values of hormone profile (glucagon, active GLP-1 and GIP) at 12 weeks of coleosoma treatment vs placebo
Description
Difference in the hormone profile compared to baseline in the 2 arms. All these parameters have the same Units of Measure (pg/ml)
Time Frame
12 weeks
Title
Change from baseline values of Endothelial Progenitor Cells (EPC) number at 12 weeks of coleosoma treatment vs placebo
Description
Difference in the EPC number compared to baseline in the 2 arms.
Time Frame
12 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
non-HDL cholesterol ≥ 160 mg/dl;
providing their written Informed Consent;
capable of understanding the nature, purpose and study procedures
Exclusion Criteria:
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;
monogenic dyslipidemia;
participation in other clinical trials in the previous 30 days;
uncompensated hypothyroidism
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alessandra Dei Cas, MD
Organizational Affiliation
University of Parma
Official's Role
Principal Investigator
Facility Information:
Facility Name
Endocrinology Unit
City
Parma
ZIP/Postal Code
43126
Country
Italy
12. IPD Sharing Statement
Plan to Share IPD
No
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Efficacy and Tolerability of the Nutraceutical Formulation Coleosoma in Dyslipidemic Subjects
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