Study Stopped
Tredaptive has been suspended worldwide
Effects of Niacin on Good Cholesterol in People With Peripheral Arterial Disease
The Effects of Chronic High-density Lipoprotein (HDL) Elevation With Extended Release Niacin on Peripheral Arterial Disease
1 other identifier
interventional
7
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jul 2011
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 5, 2011
CompletedStudy Start
First participant enrolled
July 1, 2011
CompletedFirst Posted
Study publicly available on registry
July 12, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2014
CompletedFebruary 27, 2013
February 1, 2013
3.4 years
April 5, 2011
February 25, 2013
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
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.
8 weeks after recruitment.
Secondary Outcomes (7)
Plasma Monocyte Activation
8 weeks after recruitment
Plasma Neutrophil Adhesion to Immobilized Fibrinogen
8 weeks after recruitment
Platelet Aggregation Assays
8 weeks after recruitment
Plasma Thrombotic Markers
8 weeks after recruitment
Size distribution and composition of HDL
8 weeks after recruitment
- +2 more secondary outcomes
Study Arms (2)
Niacin / Laropiprant
ACTIVE COMPARATORSugar Pill (Placebo)
PLACEBO COMPARATORInterventions
Niacin 1g / Laropiprant 20mg for 4 weeks followed by Niacin 2g / Laropiprant 20mg for 4 weeks
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Baker IDI Heart and diabetes research institute
Melbourne, Victoria, 3004, Australia
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Bronwyn Kingwell, Bsc, PhD
Baker IDI
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER GOV
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 5, 2011
First Posted
July 12, 2011
Study Start
July 1, 2011
Primary Completion
December 1, 2014
Study Completion
December 1, 2014
Last Updated
February 27, 2013
Record last verified: 2013-02