search
Back to results

Effects of Nicotinic Acid Plus Simvastatin Versus Simvastatin Alone on Carotid and Femoral Intima-Media Thickness in Patients With Peripheral Artery Disease (NASCIT) (NASCIT)

Primary Purpose

Dyslipidemia, Atherosclerosis

Status
Unknown status
Phase
Phase 4
Locations
Austria
Study Type
Interventional
Intervention
simvastatin
Nicotinic Acid
Sponsored by
Medical University of Vienna
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dyslipidemia focused on measuring intima-media-thickness, dyslipidemia, progression of atherosclerosis, peripheral artery disease, major cardiovascular events

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • PAD defined as an ABI ≤0.9 or >1.3 in patients with low serum HDL cholesterol levels (<45mg/dL in men, <55 mg/dL in women)

Exclusion Criteria:

  • Elevated liver enzymes (above 2 times the normal level)
  • Skeletal muscle myopathy or elevated serum CK levels
  • Allergy or hypersensibility to either statins or nicotinic acid
  • Women of childbearing potential

Sites / Locations

  • Medical University ViennaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

1

2

Arm Description

Nicotinic acid + Simvastatin

Simvastatin

Outcomes

Primary Outcome Measures

change of carotid and femoral IMT from baseline to 6 and 12 months follow up and occurrence of major adverse cardiovascular events (MACE)

Secondary Outcome Measures

changes of grey scale median (GSM) score from baseline to follow-up, and changes of serum levels of total cholesterol, low-density lipoprotein cholesterol (LDL-c), high-density lipoprotein cholesterol (HDL-c), triglycerides and lipoprotein (a).

Full Information

First Posted
July 3, 2008
Last Updated
July 20, 2011
Sponsor
Medical University of Vienna
search

1. Study Identification

Unique Protocol Identification Number
NCT00712049
Brief Title
Effects of Nicotinic Acid Plus Simvastatin Versus Simvastatin Alone on Carotid and Femoral Intima-Media Thickness in Patients With Peripheral Artery Disease (NASCIT)
Acronym
NASCIT
Official Title
Effects of Nicotinic Acid Plus Simvastatin Versus Simvastatin Alone on Carotid and Femoral Intima-Media Thickness in Patients With Peripheral Artery Disease (NASCIT)-A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2011
Overall Recruitment Status
Unknown status
Study Start Date
June 2008 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Medical University of Vienna

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Dyslipidaemia is characterized by low plasma levels of high-density lipoprotein cholesterol (HDL-c), elevated triglycerides and an increase in low density lipoprotein (LDL-c) particles, and has been unequivocally established as a most important cardiovascular risk factor. While statins are effective in reducing plasma levels of LDL-c, these drugs have only modest effects on raising HDL-c (typically by less than 10%), even with aggressive statin therapy. However, increasing evidence suggests that low HDL-c might be at least as relevant as high LDL-c in promoting the development and progression of atherosclerosis. The beneficial effect of raising HDL-c on clinical outcome has already been demonstrated by several studies. Nicotinic acid is the most potent agent available for raising plasma levels of HDL-c by up to 29% at clinically recommended doses, and substantially lowers triglycerides and LDL-c. Furthermore, nicotinic acid is also the most potent lipid lowering agent available that reduces Lp(a), an independent marker of cardiovascular risk. In a recent study patients with coronary artery disease had a 21% increase in HDL-c and a 13% decrease in triglycerides, and these beneficial effects on lipid status may have contributed to a stabilization or regression of carotid intima-media-thickness (IMT).The impact in patients with advanced atherosclerosis like peripheral artery disease (PAD) in unknown. The investigators hypothesized that nicotinic acid in addition to statin therapy may inhibit progression of peripheral arterial atherosclerosis. Therefore, the aim of the present randomized controlled trial is to investigate the effects of nicotinic acid (daily dose starting with 500 mg, up to 2000mg) in addition to simvastatin (40 mg daily) versus simvastatin (40mg daily) monotherapy in patients with low serum HDL-C levels and PAD with respect to changes of carotid and femoral IMT, changes of patients´ lipid status and occurrence of major adverse cardiovascular events (MACE).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dyslipidemia, Atherosclerosis
Keywords
intima-media-thickness, dyslipidemia, progression of atherosclerosis, peripheral artery disease, major cardiovascular events

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Nicotinic acid + Simvastatin
Arm Title
2
Arm Type
Active Comparator
Arm Description
Simvastatin
Intervention Type
Drug
Intervention Name(s)
simvastatin
Intervention Description
simvastatin 40 mg
Intervention Type
Drug
Intervention Name(s)
Nicotinic Acid
Intervention Description
daily dose starting with 500 mg, up to 2000mg
Primary Outcome Measure Information:
Title
change of carotid and femoral IMT from baseline to 6 and 12 months follow up and occurrence of major adverse cardiovascular events (MACE)
Time Frame
6 and 12 months
Secondary Outcome Measure Information:
Title
changes of grey scale median (GSM) score from baseline to follow-up, and changes of serum levels of total cholesterol, low-density lipoprotein cholesterol (LDL-c), high-density lipoprotein cholesterol (HDL-c), triglycerides and lipoprotein (a).
Time Frame
6 and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: PAD defined as an ABI ≤0.9 or >1.3 in patients with low serum HDL cholesterol levels (<45mg/dL in men, <55 mg/dL in women) Exclusion Criteria: Elevated liver enzymes (above 2 times the normal level) Skeletal muscle myopathy or elevated serum CK levels Allergy or hypersensibility to either statins or nicotinic acid Women of childbearing potential
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Renate Koppensteiner, Prof. Dr.
Organizational Affiliation
Division of Angiology, Department of Internal Medicine II, Medical University Vienna
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medical University Vienna
City
Vienna
ZIP/Postal Code
1090
Country
Austria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Renate Koppensteiner, Prof. Dr.
Phone
00431404004671
Email
renate.koppensteiner@meduniwien.ac.at
First Name & Middle Initial & Last Name & Degree
Martin Schillinger, Prof. Dr.
First Name & Middle Initial & Last Name & Degree
Jasmin Amighi, Dr.
First Name & Middle Initial & Last Name & Degree
Schila Sabeti, Dr.

12. IPD Sharing Statement

Learn more about this trial

Effects of Nicotinic Acid Plus Simvastatin Versus Simvastatin Alone on Carotid and Femoral Intima-Media Thickness in Patients With Peripheral Artery Disease (NASCIT)

We'll reach out to this number within 24 hrs