Overview

Niacin As Secondary Prevention Of Coronary Artery Disease (NASPOCAD)

Status:
Unknown status
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
All
Summary
Aim of the study is to show additional effects of the combined therapy of niacin and statins analyzing number and function of EPCs and other stem cell populations and adiponectin as well as hsCRP levels in patients with CAD.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Ludwig-Maximilians - University of Munich
Treatments:
Niacin
Niacinamide
Nicotinic Acids
Criteria
Inclusion Criteria:

- Be at least 18 years old, male or female

- Have stable coronary artery disease (i.e. no acute event like myocardial infarction or
PTCA less then 3 months ago)

- LDL > 100 mg/dl

- HDL < 50 mg/dl

- Triglycerides < 400 mg/dl

- No Nicotine abuse for at least 3 months

- Statin-therapy for more than 4 weeks

- Give a written informed consent

- Have the ability to understand the requirements of the study, and agree and be able to
return for the required assessments.

Exclusion Criteria:

- Women of childbearing potential, pregnancy or being lactating

- Current participation in another clinical trial

- Have other severe concurrent illness (e.g., active infection, malignancy)

- Have a history of alcohol or drug abuse within 3 months of admission or factors making
follow-up difficult or unlikely.

- Have significant or unexplained liver dysfunction or chronic increased levels of
transaminases (ALT, AST)

- Suffer from myopathy, active peptic disease or arterial bleeding

- Have a known hypersensitivity against niacin or statins

- Are actually treated with any of itraconazole, ketoconazole, HIV-Protease-Inhibitors,
erythromycin, clarithromycin, telithromycin, nefazodone.

- Actual therapy with ezetimibe

- Diabetes mellitus Type I