NCT01391377

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

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
7

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jul 2011

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
terminated

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

Completed
3 months until next milestone

Study Start

First participant enrolled

July 1, 2011

Completed
11 days until next milestone

First Posted

Study publicly available on registry

July 12, 2011

Completed
3.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2014

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2014

Completed
Last Updated

February 27, 2013

Status Verified

February 1, 2013

Enrollment Period

3.4 years

First QC Date

April 5, 2011

Last Update Submit

February 25, 2013

Conditions

Keywords

HDLHigh density LipoproteinPeripheral arterial diseaseTredaptiveNiacinLaropiprantPlaqueAtherosclerosisLipid content

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 COMPARATOR
Drug: Niacin/Laropiprant combination

Sugar Pill (Placebo)

PLACEBO COMPARATOR
Drug: Sugar pill

Interventions

Niacin 1g / Laropiprant 20mg for 4 weeks followed by Niacin 2g / Laropiprant 20mg for 4 weeks

Also known as: Tredaptive
Niacin / Laropiprant

Placebo

Also known as: Placebo
Sugar Pill (Placebo)

Eligibility Criteria

Age40 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Peripheral Arterial DiseasePlaque, AmyloidAtherosclerosis

Interventions

NiacinSugars

Condition Hierarchy (Ancestors)

ArteriosclerosisArterial Occlusive DiseasesVascular DiseasesCardiovascular DiseasesPeripheral Vascular DiseasesPathological Conditions, AnatomicalPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Nicotinic AcidsAcids, HeterocyclicHeterocyclic CompoundsPyridinesHeterocyclic Compounds, 1-RingCarbohydrates

Study Officials

  • Bronwyn Kingwell, Bsc, PhD

    Baker IDI

    PRINCIPAL INVESTIGATOR

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

Locations