Effects of Niacin on Good Cholesterol in People With Peripheral Arterial Disease
Primary Purpose
Peripheral Arterial Disease
Status
Terminated
Phase
Not Applicable
Locations
Australia
Study Type
Interventional
Intervention
Niacin/Laropiprant combination
Sugar pill
Sponsored by
About this trial
This is an interventional basic science trial for Peripheral Arterial Disease focused on measuring HDL, High density Lipoprotein, Peripheral arterial disease, Tredaptive, Niacin, Laropiprant, Plaque, Atherosclerosis, Lipid content
Eligibility Criteria
Inclusion Criteria:
- age >40 years
- ankle-brachial index (ABI) of <0.9 at rest in at least one leg,
- symptom limiting intermittent claudication (unilateral or bilateral) and stable for the previous 6 months,
- superficial femoral artery disease amenable to percutaneous revascularisation,
- serum HDL <1.0 mmol/l
- a stable medication regime for at least 6 months
Exclusion Criteria:
- acute myocardial infarction or presentation with angina within 1 month of enrolment,
- serum creatinine >0.2mmol/l,
- significant co-morbidity with expected survival <6 months,
- current niacin or fibrate therapy
- unable to give informed consent
Sites / Locations
- Baker IDI Heart and diabetes research institute
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Niacin / Laropiprant
Sugar Pill (Placebo)
Arm Description
Outcomes
Primary Outcome Measures
Plaque composition
After femoral arthrectomy the excised plaque will analysed for histological studies, for lipid content, immunohistochemistry, macrophage content and size and VCAM-1 staining.
Secondary Outcome Measures
Plasma Monocyte Activation
Cd11b expression on peripheral blood monocytes will be measured as a marker of monocyte activation.
Plasma Neutrophil Adhesion to Immobilized Fibrinogen
Platelet Aggregation Assays
Plasma Thrombotic Markers
Size distribution and composition of HDL
Ex vivo cholesterol efflux
Plasma lipid parameters and inflammatory markers
Lipid levels including total cholesterol, HDL, LDL and TGs, will be measured as well as ApoA1 protien and Plasma soluble ICAM-1 and soluble VCAM-1. TNF-A levels will also be measured and CRP.
Full Information
NCT ID
NCT01391377
First Posted
April 5, 2011
Last Updated
February 25, 2013
Sponsor
Bayside Health
Collaborators
National Health and Medical Research Council, Australia
1. Study Identification
Unique Protocol Identification Number
NCT01391377
Brief Title
Effects of Niacin on Good Cholesterol in People With Peripheral Arterial Disease
Official Title
The Effects of Chronic High-density Lipoprotein (HDL) Elevation With Extended Release Niacin on Peripheral Arterial Disease
Study Type
Interventional
2. Study Status
Record Verification Date
February 2013
Overall Recruitment Status
Terminated
Why Stopped
Tredaptive has been suspended worldwide
Study Start Date
July 2011 (undefined)
Primary Completion Date
December 2014 (Anticipated)
Study Completion Date
December 2014 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Bayside Health
Collaborators
National Health and Medical Research Council, Australia
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Atherosclerosis is a disorder in the body that is characterized by cholesterol plaque formation in various arteries, causing narrowing of the artery and a limitation in blood flow. Depending on which artery the plaque is in, different clinical conditions occur. In adults common areas include in the heart arteries, in the neck arteries and in the aorta and lower leg arteries. When it affects the lower limbs it is known as peripheral arterial disease - PAD.
The main symptom of PAD is called "claudication" and is described as pain or discomfort in the legs when walking. The aim of PAD treatment is to improve walking distance and quality of life in those with intermittent claudication, and to decrease long term complications including illness and death.
An important controlling factor of these cholesterol plaques is a type of cholesterol called HDL (High density lipoprotein).
This study aims to look at the effect that raising HDL for a prolonged period has on blood markers of inflammation and on the cholesterol plaque composition in patients with PAD. This investigation will also have relevance to the effects of HDL elevation on plaque composition and inflammation in other areas of the body including the heart, neck and brain arteries.
Twenty (20) PAD patients with will be recruited into the study. The investigators anticipate recruitment of all 20 patients within 12 months. The 20 PAD patients all must have significant leg pains when walking, and after review by a doctor, be determined to have narrowings in the leg artery that they will plan to operate on. Patients will be randomized to either niacin (Tredaptive, 1g/day) or matching placebo for 8 weeks (prior to operation) After the 8 week period they will then go on to receive the normal interventional treatment as planned. Blood samples will be taken at enrollment and at the 8 week mark prior to surgery. The plaque that is removed at the time of operation will also be sent to the lab for analysis.
The investigators hope to show with this study that by raising the levels of HDL with extended release niacin, there are positive effects on the amount of cholesterol in the plaque, and on the markers in the blood of inflammation and thrombosis.
The hypothesis is that elevation of HDL with Niacin will have anti-atherosclerotic actions including: Lower plaque lipid content, Reduced plaque macrophage infiltration, Reduced monocyte activation, Reduced neutrophil adhesion, Inhibition of inflammation and Inhibition of thrombotic markers.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Arterial Disease
Keywords
HDL, High density Lipoprotein, Peripheral arterial disease, Tredaptive, Niacin, Laropiprant, Plaque, Atherosclerosis, Lipid content
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
7 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Niacin / Laropiprant
Arm Type
Active Comparator
Arm Title
Sugar Pill (Placebo)
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Niacin/Laropiprant combination
Other Intervention Name(s)
Tredaptive
Intervention Description
Niacin 1g / Laropiprant 20mg for 4 weeks followed by Niacin 2g / Laropiprant 20mg for 4 weeks
Intervention Type
Drug
Intervention Name(s)
Sugar pill
Other Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
Plaque composition
Description
After femoral arthrectomy the excised plaque will analysed for histological studies, for lipid content, immunohistochemistry, macrophage content and size and VCAM-1 staining.
Time Frame
8 weeks after recruitment.
Secondary Outcome Measure Information:
Title
Plasma Monocyte Activation
Description
Cd11b expression on peripheral blood monocytes will be measured as a marker of monocyte activation.
Time Frame
8 weeks after recruitment
Title
Plasma Neutrophil Adhesion to Immobilized Fibrinogen
Time Frame
8 weeks after recruitment
Title
Platelet Aggregation Assays
Time Frame
8 weeks after recruitment
Title
Plasma Thrombotic Markers
Time Frame
8 weeks after recruitment
Title
Size distribution and composition of HDL
Time Frame
8 weeks after recruitment
Title
Ex vivo cholesterol efflux
Time Frame
8 weeks after recruitment
Title
Plasma lipid parameters and inflammatory markers
Description
Lipid levels including total cholesterol, HDL, LDL and TGs, will be measured as well as ApoA1 protien and Plasma soluble ICAM-1 and soluble VCAM-1. TNF-A levels will also be measured and CRP.
Time Frame
8 weeks after recruitment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
age >40 years
ankle-brachial index (ABI) of <0.9 at rest in at least one leg,
symptom limiting intermittent claudication (unilateral or bilateral) and stable for the previous 6 months,
superficial femoral artery disease amenable to percutaneous revascularisation,
serum HDL <1.0 mmol/l
a stable medication regime for at least 6 months
Exclusion Criteria:
acute myocardial infarction or presentation with angina within 1 month of enrolment,
serum creatinine >0.2mmol/l,
significant co-morbidity with expected survival <6 months,
current niacin or fibrate therapy
unable to give informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bronwyn Kingwell, Bsc, PhD
Organizational Affiliation
Baker IDI
Official's Role
Principal Investigator
Facility Information:
Facility Name
Baker IDI Heart and diabetes research institute
City
Melbourne
State/Province
Victoria
ZIP/Postal Code
3004
Country
Australia
12. IPD Sharing Statement
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Effects of Niacin on Good Cholesterol in People With Peripheral Arterial Disease
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