search
Back to results

Study of Niacin and Rosiglitazone in Dysmetabolic Dyslipidemia

Primary Purpose

Metabolic Syndrome X, Insulin Resistance

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
fenofibrate
niacin
rosiglitazone
Sponsored by
Foundation Research, Florida
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Metabolic Syndrome X focused on measuring fenofibrate, niacin, rosiglitazone, LDL phenotype pattern B, small, dense LDL, insulin resistance, Metabolic Syndrome

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Age >= 18 years Fasting triglycerides > 100 mg/dL Fasting plasma glucose 110-128 mg/dL Non-pattern A LDL phenotype Exclusion Criteria: Overt diabetes mellitus Current therapy with hypoglycemic agents Secondary causes of dyslipidemia (e.g. HRT, thyroid disease) Serum creatinine > 2.5 mg/dL or nephrotic syndrome AST/ALT > 3X upper limits of normal Known gallbladder disease History of gout or hyperuricemia History of peptic ulcer disease Hypersensitivity or intolerance to any of the study drugs Women who are pregnant or nursing

Sites / Locations

  • Foundation Research

Outcomes

Primary Outcome Measures

The effect of treatment on Peak LDL particle size

Secondary Outcome Measures

The effect of treatment on:
traditional lipid parameters (LDL-C, HDL-C, triglycerides)
% of lipids in regions IIIa+IIIb of a gradient gel electrophoresis
LDL phenotype
fasting glucose
Hemoglobin A1c

Full Information

First Posted
March 17, 2006
Last Updated
March 17, 2006
Sponsor
Foundation Research, Florida
Collaborators
GlaxoSmithKline, Kos Pharmaceuticals, Abbott
search

1. Study Identification

Unique Protocol Identification Number
NCT00304993
Brief Title
Study of Niacin and Rosiglitazone in Dysmetabolic Dyslipidemia
Official Title
Study of Niacin and Rosiglitazone in Dysmetabolic Dyslipidemia
Study Type
Interventional

2. Study Status

Record Verification Date
March 2006
Overall Recruitment Status
Completed
Study Start Date
January 2001 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
February 2005 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Foundation Research, Florida
Collaborators
GlaxoSmithKline, Kos Pharmaceuticals, Abbott

4. Oversight

5. Study Description

Brief Summary
Lipid abnormalities in people with the Metabolic Syndrome (the Insulin Resistance Syndrome) are characterized by elevations in triglycerides and LDL cholesterol; low levels of HDL cholesterol; and small, dense LDL particles. Statins generally do not change LDL particle size, so often fenofibrate is added. This combination may still not be sufficient. Niacin is a common third drug added to the treatment regimen, but niacin can increase insulin resistance. This study compares niacin as a third drug to rosiglitazone, an insulin sensitizer.
Detailed Description
The Metabolic Syndrome is characterized by an atherogenic dyslipidemia consisting of hypertriglyceridemia, modest elevations of LDL cholesterol, low levels of HDL cholesterol, and LDL phenotype pattern B (small, dense LDL particles). Statins are first line therapy, and reduce LDL cholesterol levels without affecting LDL particle size. Fenofibrate addresses the triglycerides, HDL cholesterol levels, and LDL phenotype, so is recommended as second level therapy. The third element is niacin, but for insulin resistant patients, a question has been whether niacin might be exacerbating the underlying pathophysiology of Metabolic Syndrome patients. In SNARED, niacin was compared to the insulin sensitizer rosiglitazone in study subjects already on statin and fenofibrate. All volunteers participating in SNARED exhibit LDL phenotype pattern B despite statin therapy at the time of recruitment. Comparisons of LDL phenotype at baseline are to be compared to measurements made after 4 months of statin + fenofibrate. If the LDL phenotype converts to pattern A (large LDL particles), this is a study endpoint. Otherwise, study subjcts are randomized to receive statin+fenofibrate+niacin, or statin+fenofibrate+rosiglitazone for six months, at which time lipid phenotype will again be determined..

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metabolic Syndrome X, Insulin Resistance
Keywords
fenofibrate, niacin, rosiglitazone, LDL phenotype pattern B, small, dense LDL, insulin resistance, Metabolic Syndrome

7. Study Design

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

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
fenofibrate
Intervention Type
Drug
Intervention Name(s)
niacin
Intervention Type
Drug
Intervention Name(s)
rosiglitazone
Primary Outcome Measure Information:
Title
The effect of treatment on Peak LDL particle size
Secondary Outcome Measure Information:
Title
The effect of treatment on:
Title
traditional lipid parameters (LDL-C, HDL-C, triglycerides)
Title
% of lipids in regions IIIa+IIIb of a gradient gel electrophoresis
Title
LDL phenotype
Title
fasting glucose
Title
Hemoglobin A1c

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age >= 18 years Fasting triglycerides > 100 mg/dL Fasting plasma glucose 110-128 mg/dL Non-pattern A LDL phenotype Exclusion Criteria: Overt diabetes mellitus Current therapy with hypoglycemic agents Secondary causes of dyslipidemia (e.g. HRT, thyroid disease) Serum creatinine > 2.5 mg/dL or nephrotic syndrome AST/ALT > 3X upper limits of normal Known gallbladder disease History of gout or hyperuricemia History of peptic ulcer disease Hypersensitivity or intolerance to any of the study drugs Women who are pregnant or nursing
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael E McIvor, MD
Organizational Affiliation
Foundation Research
Official's Role
Principal Investigator
Facility Information:
Facility Name
Foundation Research
City
St. Petersburg
State/Province
Florida
ZIP/Postal Code
33705
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Study of Niacin and Rosiglitazone in Dysmetabolic Dyslipidemia

We'll reach out to this number within 24 hrs