Atorvastatin and Endothelial Function in Type 2 Diabetes Mellitus (ATTEND-Study)
Primary Purpose
Type 2 Diabetes Mellitus
Status
Completed
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Atorvastatin
Sponsored by

About this trial
This is an interventional prevention trial for Type 2 Diabetes Mellitus
Eligibility Criteria
Inclusion Criteria: Type 2 diabetes mellitus, Total cholesterol <6.5 mmol/l Signed informed consent Exclusion Criteria: Documented CAD or peripheral vascular disease Treatment with lipid-lowering drugs Contraindications to HMG-CoA reductase therapy Potential noncompliance
Sites / Locations
- Department of Medical Research
Outcomes
Primary Outcome Measures
Flow mediated vasodilatation (FMD) on atorvastatin
Secondary Outcome Measures
FMD on combined treatment
FMD in relation to lipid levels
FMD in relation to BP lowering
CV events
Full Information
NCT ID
NCT00124397
First Posted
July 26, 2005
Last Updated
August 4, 2005
Sponsor
University of Southern Denmark
Collaborators
Pfizer
1. Study Identification
Unique Protocol Identification Number
NCT00124397
Brief Title
Atorvastatin and Endothelial Function in Type 2 Diabetes Mellitus (ATTEND-Study)
Official Title
Effect of High Dose Statin Therapy on Endothelial Function in Patients With Type 2 Diabetes Mellitus Without CAD
Study Type
Interventional
2. Study Status
Record Verification Date
July 2005
Overall Recruitment Status
Completed
Study Start Date
July 2001 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
December 2004 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
University of Southern Denmark
Collaborators
Pfizer
4. Oversight
5. Study Description
Brief Summary
The aim of this study is to examine the effect of intensive cholesterol lowering therapy and tight blood pressure (BP) regulation on endothelial function (inner cell layer of vessels that determines dilatation) in type 2 diabetic patients without documented cardiovascular (CV) disease. The hypothesis is that intensive cholesterol lowering and tight blood pressure regulation will due better than a control group.
Detailed Description
Background:The prevalence of diagnosed type 2 diabetes mellitus (DM) is estimated to 2-4% in the general population in most European countries. DM is associated with an increased frequency of manifest atherosclerotic disease. Data from prospective studies demonstrate that the risk of developing acute coronary syndrome (ACS) in diabetic patients with no prior history of coronary artery disease (CAD) is equivalent to the risk observed in non-diabetics ACS survivors. Most diabetic patients die from CAD. Although DM is primarily a metabolic disorder, it imposes a tremendous burden on macro- and micro-vessel disease.The important question of primary prevention of cardiovascular disease (CVD) in DM remains unanswered.
In the major lipid-intervention studies where patients with CAD were included, the subgroup with DM had at least as good effect of lipid lowering therapy with statins as non-diabetics. The recently published Heart Protection Study supports the hypothesis of a favourable effect of statins in the primary prevention of CVD in DM. The UK Prospective Diabetic Study has proved that tight blood pressure (BP) regulation reduces the frequency of micro- and macrovascular endpoint. It has been suggested that combined lipid lowering with statins and tight BP regulation can have an additive effect in DM patients.
It is well established that the atherosclerotic process has an impact on endothelial function.An improvement of endothelial function by cholesterol lowering and BP reduction may serve as a surrogate endpoint for CAD.
Objective:To assess the effect of intensive lipid lowering on endothelial function in patients with DM and serum cholesterol level <6.5 mmol/l and to evaluate the effect of combined lipid lowering and tight BP regulation on endothelial function in the same patient group.
Methods: This is a single-center, randomised, placebo-controlled study with three treatment arms. Participants are blindly allocated to: 1. atorvastatin 80 mg daily 2. corresponding placebo 3. open label treatment with atorvastatin 80 mg daily and tight BP regulation with 5-10 mg amlodipine, 2-4 mg perindopril, 4-8 mg doxazosin in mono- or combination therapy that aims BP <130/80.
Endothelial function is evaluated at baseline, at 6 and 12 month non-invasively. A high resolution ultrasound scan is performed on the right brachial artery to assess post ischemic flow mediated changes in arterial diameter. Flow mediated dilatation (FMD) depends on an intact endothelium and is mediated via endogenous nitric oxid (NO). To test non-endothelium dependent vasodilatation 0.4 mg of sublingual nitroglycerin (NG) is administrated. NG is a smooth muscle relaxant and acts as a source of NO.There is a well described relation tween endothelial function in the coronary arteries and in the brachial artery.
Sample size: the sample size in the study is based on the following assumptions:
High resolution ultrasound technique has a high accuracy and reproducibility.
The majority of the patients will have endothelial dysfunction
As shown in previous clinical studies, an increase in FMD of 2% is significant at the 95% confidence interval.
Patients randomised to atorvastatin will after one year treatment show an improvement of FMD of at leat 2% compared with the placebo group. Patients treated openly with atorvastatin and BP regulation will have a further improvement of FMD of 2%.
Under these assumptions with a power of 80% and a 2 sided alfa of 5% a sample size of 160 patients are needed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes Mellitus
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
186 (false)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Atorvastatin
Primary Outcome Measure Information:
Title
Flow mediated vasodilatation (FMD) on atorvastatin
Secondary Outcome Measure Information:
Title
FMD on combined treatment
Title
FMD in relation to lipid levels
Title
FMD in relation to BP lowering
Title
CV events
10. Eligibility
Sex
All
Minimum Age & Unit of Time
0 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Type 2 diabetes mellitus,
Total cholesterol <6.5 mmol/l
Signed informed consent
Exclusion Criteria:
Documented CAD or peripheral vascular disease
Treatment with lipid-lowering drugs
Contraindications to HMG-CoA reductase therapy
Potential noncompliance
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kenneth Egstrup, MD
Organizational Affiliation
Department of Medical Research, SHF Svendborg
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Medical Research
City
SHF Svendborg
State/Province
Svendborg
ZIP/Postal Code
5700
Country
Denmark
12. IPD Sharing Statement
Learn more about this trial
Atorvastatin and Endothelial Function in Type 2 Diabetes Mellitus (ATTEND-Study)
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