Omacor for the Treatment of Vascular Dysfunction in Patients With Type 2 Diabetes Mellitus
Primary Purpose
Atherosclerosis, Type 2 Diabetes Mellitus
Status
Completed
Phase
Phase 4
Locations
Germany
Study Type
Interventional
Intervention
Omacor
Sponsored by
About this trial
This is an interventional treatment trial for Atherosclerosis focused on measuring flow-mediated vasodilatation, endothelial dysfunction, omega-3 fatty acids, type 2 diabetes mellitus, postprandial state
Eligibility Criteria
Inclusion Criteria: Type 2 diabetes mellitus Exclusion Criteria: History of myocardial infarction, stroke Severe diabetes complications Severe hypo- or hypertension Chronic alcohol abuse Renal failure
Sites / Locations
- Heart- and Diabetes Centre NRW, Diabetes Clinic
Outcomes
Primary Outcome Measures
Postprandial (2, 4 and 6 hours) flow-mediated vasodilation after a 6-week treatment with Omacor
Secondary Outcome Measures
Baseline flow-mediated vasodilation after a 6-week treatment with Omacor
Full Information
NCT ID
NCT00328536
First Posted
May 19, 2006
Last Updated
May 7, 2009
Sponsor
Ruhr University of Bochum
Collaborators
Heart and Diabetes Center North-Rhine Westfalia, Solvay Pharmaceuticals
1. Study Identification
Unique Protocol Identification Number
NCT00328536
Brief Title
Omacor for the Treatment of Vascular Dysfunction in Patients With Type 2 Diabetes Mellitus
Official Title
Effects of Treatment With Omacor for 6 Weeks on Preprandial and Postprandial Endothelial Function Following a High Fat Meal in Patients With Type 2 Diabetes Mellitus
Study Type
Interventional
2. Study Status
Record Verification Date
May 2009
Overall Recruitment Status
Completed
Study Start Date
April 2007 (undefined)
Primary Completion Date
November 2008 (Actual)
Study Completion Date
November 2008 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Ruhr University of Bochum
Collaborators
Heart and Diabetes Center North-Rhine Westfalia, Solvay Pharmaceuticals
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of the study is to determine whether a 6-week treatment with 4 g Omacor/day improves the baseline and postprandial endothelial function (after a high-fat meal) in patients with type 2 diabetes mellitus.
Detailed Description
Patients with type 2 diabetes mellitus (T2DM) have a 2 to 5-fold increase in cardiovascular mortality compared to non-diabetics.
Endothelial dysfunction (ED) is an early messenger of atherosclerosis and is present in states showing a high cardiovascular (CV) risk, such as active and passive smoking, dyslipidemia, arterial hypertension, obesity, hyperhomocysteinemia, coronary artery disease, congestive heart failure and type 1 and type 2 diabetes mellitus. Endothelial function is a variable with a large day-to-day variation and shows great excursions even within one day. Several factors might play a role such as hormonal status, physical activity, sleep quality, but the most important seems to be the postprandial state. Postprandial ED was demonstrated not only in patients with CV disease or diabetes, but even in healthy subjects. A large body of evidence has accumulated showing distinctive and cumulative effects of hyperglycemia and hypertriglyceridemia on postprandial ED. Since postprandial dysmetabolism was linked to CVD, ED was proposed to be the mechanism connecting them. Considering that the postprandial state covers most of our daytime, interventions targeting a reduction in postprandial ED might play a decisive role in atherosclerosis prevention.
For the treatment of postprandial ED several therapeutical approaches have been suggested such as folic acid, tetrahydrobiopterin, vitamins C and E and statins.
Some properties of omega-3 fatty acids suggest that such an impairment of postprandial endothelial dysfunction could be prevented by treatment with Omacor® and the purpose of our study is to demonstrate that a six-week therapy with Omacor prevents endothelial dysfunction in fasting state and following a high-fat meal.
Several controlled clinical studies conducted in persons with TM2DM or after myocardial infarction have shown that consumption of omega-3 long chain polyunsaturated fatty acids (n-3 PUFA) have several beneficial effects such as: lowers risk of primary cardiac arrest, reduces triglyceride levels, increases high-density lipoprotein levels, reduces platelet aggregability, acts anti-inflammatory and immune-modulating, lowers blood pressure and improves endothelial function.
Consumption of n-3 fatty acids was shown to positively influence platelet, fibrinolytic and vascular function in hypertensive type 2 diabetic patients. Mediterranean- style diet restores markers of endothelial dysfunction and inflammation in persons with metabolic syndrome and improves endothelial function in hypercholesterolemic men.
Since Omacor contains in high-dose purified n-3 fatty acids eicosapentaenoic and docosahexaenoic acid (EPA and DHA), our first hypothesis is that a 6-week therapy with 4g/d Omacor improves fasting endothelial function in persons with T2DM.
In patients with T2DM, a three-week diet with a high amount of polyunsaturated fatty acids compared to a diet with a high amount of monounsaturated fatty acids, produces a significantly lower increase in postprandial lipemia after an oral fat load. Since postprandial lipemia induces transient endothelial dysfunction, our second hypothesis is that treatment with Omacor prevents postprandial impairment of endothelial function after a high fat meal.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atherosclerosis, Type 2 Diabetes Mellitus
Keywords
flow-mediated vasodilatation, endothelial dysfunction, omega-3 fatty acids, type 2 diabetes mellitus, postprandial state
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
Double
Allocation
Randomized
Enrollment
34 (Anticipated)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Omacor
Primary Outcome Measure Information:
Title
Postprandial (2, 4 and 6 hours) flow-mediated vasodilation after a 6-week treatment with Omacor
Secondary Outcome Measure Information:
Title
Baseline flow-mediated vasodilation after a 6-week treatment with Omacor
10. Eligibility
Sex
All
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Type 2 diabetes mellitus
Exclusion Criteria:
History of myocardial infarction, stroke
Severe diabetes complications
Severe hypo- or hypertension
Chronic alcohol abuse
Renal failure
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Diethelm Tschoepe, MD, Prof.
Organizational Affiliation
Heart and Diabetes Center North-Rhine Westfalia
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Alin Stirban, MD
Organizational Affiliation
Heart and Diabetes Center North-Rhine Westfalia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Heart- and Diabetes Centre NRW, Diabetes Clinic
City
Bad Oeynhausen
State/Province
NRW
ZIP/Postal Code
32545
Country
Germany
12. IPD Sharing Statement
Citations:
PubMed Identifier
24356795
Citation
Stirban A, Nandrean S, Gotting C, Stratmann B, Tschoepe D. Effects of n-3 polyunsaturated fatty acids (PUFAs) on circulating adiponectin and leptin in subjects with type 2 diabetes mellitus. Horm Metab Res. 2014 Jun;46(7):490-2. doi: 10.1055/s-0033-1363225. Epub 2013 Dec 19.
Results Reference
derived
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Omacor for the Treatment of Vascular Dysfunction in Patients With Type 2 Diabetes Mellitus
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