Armolipid Plus and Metabolic Syndrome
Primary Purpose
Metabolic Syndrome
Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Armolipid Plus
Sponsored by
About this trial
This is an interventional treatment trial for Metabolic Syndrome focused on measuring Metabolic Syndrome Insulin-resistance Endothelial Function
Eligibility Criteria
Inclusion Criteria:
Male and Female 18-65 aged, with diagnosis of metabolic syndrome, defined by the presence of waist circumference > 102 cm (M) or >88 cm(F), and two or more of these criteria:
- fasting blood glucose >100 mg;
- systolic blood pressure >135 or diastolic blood pressure >85 mmHg or patients in treatment with antihypertensive drugs;
- triglyceridemia >150 mg/dl;
- HDL cholesterolemia < 40 mg/dl(M), < 50 mg/dl(F).
Exclusion Criteria:
- pregnancy
- diabetes mellitus in pharmacologic treatment;
- hepatic failure;
- creatininemia >2 mg/dl;
- triglyceridemia > 500 mg/dl;
- heart failure.
Sites / Locations
- Federico II University - Department of Internal Medicine
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Armolipid Plus
Placebo
Arm Description
Armolipid Plus is an association of berberine 500 mg, red yeast rice titled in 3 mg monacolin K,- policosanol 10 mg,coenzyme Q10 2 mg,astaxanthin 0,5 mg,folic acid 0,2 mg
Placebo matching Armolipid plus
Outcomes
Primary Outcome Measures
Insulin/glucose ratio after overnight fast
HOMA INDEX
Insuline/glucose ratio after an oralglucose tolerance test
OGTT
Secondary Outcome Measures
BMI
evaluation of weight and BMI
Glycemia
Blood Glucose
Endothelial function
endothelial function assessed by Flow Mediated Dilation
C reactive protein.
dosage of CRP
Serum lipidemia
measure of TG and cholesterol
Full Information
NCT ID
NCT01087632
First Posted
March 12, 2010
Last Updated
September 1, 2010
Sponsor
Rottapharm
Collaborators
Federico II University
1. Study Identification
Unique Protocol Identification Number
NCT01087632
Brief Title
Armolipid Plus and Metabolic Syndrome
Official Title
Effects of Armolipid Plus on Indices of Insulin Resistance in Patients With Metabolic Syndrome
Study Type
Interventional
2. Study Status
Record Verification Date
September 2010
Overall Recruitment Status
Completed
Study Start Date
September 2009 (undefined)
Primary Completion Date
July 2010 (Actual)
Study Completion Date
July 2010 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Rottapharm
Collaborators
Federico II University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Metabolic syndrome is a highly prevalent condition characterized by visceral obesity, abnormalities of glucidic and lipid metabolism, and increased risk for cardiovascular events. Such findings appear to be associated with a decrease in insulin sensitivity. Management of metabolic syndrome is currently aimed at treating individual components of the disease without addressing this underlying pathophysiologic mechanism; this translates into multidrug regimens, high costs and patient compliance issues.
Armolipid Plus (an association of berberine 500 mg, red yeast rice titled in 3 mg monacolin K,policosanol 10 mg,coenzyme Q10 2 mg,astaxanthin 0,5 mg,folic acid 0,2 mg) has been found to be effective at reducing blood cholesterol and triglycerides, and at improving endothelial function; subgroup analyses also suggested a benefit on indices of insulin resistance.
Aim of the study is to evaluate the effects of Armolipid Plus on insulin sensitivity and on the diagnostic parameters of metabolic syndrome.
60 patients will be enrolled in this randomized, double-blind, placebo-controlled trial; active treatment will consist of Armolipid Plus (1 tbl qd).
Primary end point will be the reduction of the insulin/glucose ratio, both after overnight fast (HOMA index) and after an oral glucose tolerance test (OGTT).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metabolic Syndrome
Keywords
Metabolic Syndrome Insulin-resistance Endothelial Function
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
66 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Armolipid Plus
Arm Type
Experimental
Arm Description
Armolipid Plus is an association of berberine 500 mg, red yeast rice titled in 3 mg monacolin K,- policosanol 10 mg,coenzyme Q10 2 mg,astaxanthin 0,5 mg,folic acid 0,2 mg
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo matching Armolipid plus
Intervention Type
Dietary Supplement
Intervention Name(s)
Armolipid Plus
Other Intervention Name(s)
berberine, red yeast rice, monacolin K, policosanol, coenzyme Q10, astaxanthin, folic acid
Intervention Description
Armolipid Plus 1 tablet QD for 18 weeks
Primary Outcome Measure Information:
Title
Insulin/glucose ratio after overnight fast
Description
HOMA INDEX
Time Frame
18 weeks
Title
Insuline/glucose ratio after an oralglucose tolerance test
Description
OGTT
Time Frame
18 weeks
Secondary Outcome Measure Information:
Title
BMI
Description
evaluation of weight and BMI
Time Frame
18 weeks
Title
Glycemia
Description
Blood Glucose
Time Frame
18 weeks
Title
Endothelial function
Description
endothelial function assessed by Flow Mediated Dilation
Time Frame
18 weeks
Title
C reactive protein.
Description
dosage of CRP
Time Frame
18 weeks
Title
Serum lipidemia
Description
measure of TG and cholesterol
Time Frame
18 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Male and Female 18-65 aged, with diagnosis of metabolic syndrome, defined by the presence of waist circumference > 102 cm (M) or >88 cm(F), and two or more of these criteria:
fasting blood glucose >100 mg;
systolic blood pressure >135 or diastolic blood pressure >85 mmHg or patients in treatment with antihypertensive drugs;
triglyceridemia >150 mg/dl;
HDL cholesterolemia < 40 mg/dl(M), < 50 mg/dl(F).
Exclusion Criteria:
pregnancy
diabetes mellitus in pharmacologic treatment;
hepatic failure;
creatininemia >2 mg/dl;
triglyceridemia > 500 mg/dl;
heart failure.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Serafino Fazio, MD
Organizational Affiliation
Federico II University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Federico II University - Department of Internal Medicine
City
Naples
Country
Italy
12. IPD Sharing Statement
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Armolipid Plus and Metabolic Syndrome
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