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SLIM: Combined Effects of Slo-Niacin and Atorvastatin on Lipoproteins and Inflammatory Markers in Hyperlipidemia

Primary Purpose

Dyslipidemia

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Slo-Niacin, atorvastatin
Sponsored by
University of Washington
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dyslipidemia focused on measuring cholesterol, dyslipidemia, hypercholesterolemia, C-reactive protein

Eligibility Criteria

21 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: LDL-C > 130 mg/dL HDL-C <= 45 mg/dL in men and <= 55 mg/dL in women Exclusion Criteria: history of hypersensitivity to any statin, niacin or aspirin diagnosis of diabetes or a fasting glucose > 125 mg/dL hyper or hypothyroidism (unless treatment stable) meet other health, medication, and logistical criteria

Sites / Locations

  • Northwest Lipid Research Clinic, University of Washington

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

1

2

Arm Description

Atorvastatin 10 mg for 12 weeks followed by Slo-Niacin (titrated from 500 to 1500 mg over 8 weeks) taken with atorvastatin 10 mg for an additional 12 weeks

Slo-Niacin (titrated from 500 to 1500 mg over 8 weeks) for 12 weeks followed by atorvastatin 10 mg taken with Slo-Niacin 1500 mg for an additional 12 weeks

Outcomes

Primary Outcome Measures

LDL-C change for atorvastatin 10 mg, Slo-Niacin 1500 mg, and the two together.

Secondary Outcome Measures

Change in HDL-C, HDL2-C, HDL3-C, LDL-C:HDL-C, triglyceride, remnant lipoprotein, apoproteins A-I and B, LDL buoyancy, hsCRP, glucose, insulin, and SGOT.

Full Information

First Posted
September 12, 2005
Last Updated
August 20, 2008
Sponsor
University of Washington
Collaborators
Upsher-Smith Laboratories
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1. Study Identification

Unique Protocol Identification Number
NCT00194402
Brief Title
SLIM: Combined Effects of Slo-Niacin and Atorvastatin on Lipoproteins and Inflammatory Markers in Hyperlipidemia
Official Title
SLIM: Combined Effects of Slo-Niacin and Atorvastatin on Lipoproteins and Inflammatory Markers
Study Type
Interventional

2. Study Status

Record Verification Date
August 2008
Overall Recruitment Status
Completed
Study Start Date
August 2003 (undefined)
Primary Completion Date
January 2006 (Actual)
Study Completion Date
January 2006 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University of Washington
Collaborators
Upsher-Smith Laboratories

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Slo-Niacin and atorvastatin (Lipitor) are both drugs that lower cholesterol. In this research, we will compare the effectiveness of Slo-Niacin and atorvastatin taken alone and together. This study will help show how the individual benefits of the two drugs taken separately can be combined when taken together.
Detailed Description
Combined niacin and a statin treatment has greater potential value than either agent alone for the dyslipidemia of insulin resistance, obesity and the metabolic syndrome. The efficacy of Slo-Niacin and atorvastatin has not been formally examined in this setting. Methods: Forty-four dyslipidemic men and women (LDL-C >130mg/dL and below average HDL-C (<55 in women and <45 in men) were randomized to a 3 month course of atorvastatin 10 mg or Slo-Niacin increased monthly at doses of 500, 1000 and 1500 mg/day. The alternate drug was added in the second 3-month segment. Lipid profiles and transaminase measurements were obtained monthly and full lipoprotein quantifications, apoproteins, remnant like lipoproteins (RLP), LDL buoyancy, glucose, insulin, and C-reactive protein were measured at the end of each 3-month sequence. Results: Mean entry lipids were (mg/dL) TG 187, LDL-C 171, HDL-C 39. Mean BMI was 32.6 Kg/M2. When Slo-Niacin and atorvastatin were given alone, respective decreases in triglyceride (TG) were 18% and 10%, LDL-C 12% and 36% and non-HDL-C 15% and 36%. HDL-C increased 8% and 6%, respectively. Combined therapy decreased median TG 33% and mean LDL-C 43% and increased mean HDL-C 10%. Mean hs CRP decreased 23% and RLP 44.5% in the combined groups. Conclusions: Slo-Niacin with atorvastatin improves all lipoprotein fractions, RLP and hsCRP in combined hyperlipidemia. The reduction of LDL with the drug combination is equivalent to that obtained with 20-80 mg of atorvastatin alone.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dyslipidemia
Keywords
cholesterol, dyslipidemia, hypercholesterolemia, C-reactive protein

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Atorvastatin 10 mg for 12 weeks followed by Slo-Niacin (titrated from 500 to 1500 mg over 8 weeks) taken with atorvastatin 10 mg for an additional 12 weeks
Arm Title
2
Arm Type
Active Comparator
Arm Description
Slo-Niacin (titrated from 500 to 1500 mg over 8 weeks) for 12 weeks followed by atorvastatin 10 mg taken with Slo-Niacin 1500 mg for an additional 12 weeks
Intervention Type
Drug
Intervention Name(s)
Slo-Niacin, atorvastatin
Other Intervention Name(s)
Lipitor (R) (Atorvastatin), Slo-Niacin (R) (time-release niacin
Intervention Description
Atorvastatin 10 mg qd for 12 or 24 weeks. Time-released niacin 1500 mg qd (titrated from 500mg to 1000mg and then to 1500 mg at 4 week intervals) taken for 12 or 24 weeks.
Primary Outcome Measure Information:
Title
LDL-C change for atorvastatin 10 mg, Slo-Niacin 1500 mg, and the two together.
Time Frame
Change from baseline to 12 weeks and end of intervention
Secondary Outcome Measure Information:
Title
Change in HDL-C, HDL2-C, HDL3-C, LDL-C:HDL-C, triglyceride, remnant lipoprotein, apoproteins A-I and B, LDL buoyancy, hsCRP, glucose, insulin, and SGOT.
Time Frame
Change from baseline to end of 12 weeks and/or end of intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: LDL-C > 130 mg/dL HDL-C <= 45 mg/dL in men and <= 55 mg/dL in women Exclusion Criteria: history of hypersensitivity to any statin, niacin or aspirin diagnosis of diabetes or a fasting glucose > 125 mg/dL hyper or hypothyroidism (unless treatment stable) meet other health, medication, and logistical criteria
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert H. Knopp, MD
Organizational Affiliation
Northwest Lipid Research Clinic, University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northwest Lipid Research Clinic, University of Washington
City
Seattle
State/Province
Washington
ZIP/Postal Code
98104
Country
United States

12. IPD Sharing Statement

Learn more about this trial

SLIM: Combined Effects of Slo-Niacin and Atorvastatin on Lipoproteins and Inflammatory Markers in Hyperlipidemia

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