Evaluation of the Effect of NICOtinic Acid (Niacin) on Elevated Lipoprotein(a) Levels (NICOLa Study)
Information source: Charite University, Berlin, Germany
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Elevated Lipoprotein(a) Levels
Intervention: Nicotinic acid (niacin) (Drug); Placebo (Drug)
Phase: Phase 3
Status: Active, not recruiting
Sponsored by: Charite University, Berlin, Germany Official(s) and/or principal investigator(s): Elisabeth Steinhagen-Thiessen, MD, Study Director, Affiliation: Lipidambulanz und Lipidapherese, Charité Campus Virchow-Klinikum
Summary
Lipoprotein (Lp)(a) has been associated with increased risk of cardiovascular disease.
Niacin has been shown to lower Lp(a) in patients with normal or moderately elevated levels.
However, there are few studies assessing the effectiveness of niacin in Lp(a) levels above
30 mg/dl. In addition, most studies investigating the effectiveness of niacin have only
included small numbers of patients. Also, Lp(a) was only assessed as a secondary endpoint.
The aim of the present study was, therefore, to evaluate whether Niacin is effective
compared to placebo in the reduction of an elevated Lp(a).
Clinical Details
Official title: Evaluation of the Effect of NICOtinic Acid (Niacin) on Elevated Lipoprotein(a) Levels (NICOLa Study)
Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Primary outcome: Mean change in Lp(a) levels
Secondary outcome: Mean change in total cholesterol levelsMean change in LDL (low density lipoprotein) cholesterol levels Mean change in HDL (high density lipoprotein) cholesterol levels Mean change in triglyceride levels Mean change in blood glucose levels Health-related quality of life Disease-related costs Clinical adverse events Laboratory safety parameters Adherence to medication Tolerability of medication
Detailed description:
The study is a randomised, multicentre, placebo-controlled, 2-arm, parallel group, phase
III, intervention study. Following randomisation at visit 1, subjects will receive 20 weeks
of treatment with niacin or placebo.
The research question is: niacin therapy effective in lowering elevated Lipoprotein (Lp)(a)
levels in comparison to placebo?
Sample size calculation is based on the t test of equal means with unequal group size
(ratio: treatment group / control group = 2: 1). The significance level is α=0. 05 and the
power 90%. Assuming a drop-out rate of 20%, sample size is 100 in the niacin group and 50 in
the placebo group.
The active ingredient in the modified (prolonged, extended) release tablets is nicotinic
acid, a B-complex vitamin. Modified release tablets containing 500 mg nicotinic acid, once
daily for oral use, will be used. te of 20%, sample size is 100 in the niacin group and 50 in
the placebo group.
Subjects will be recruited consecutively in the participating lipid clinics.
Subjects will be assessed at week - 4 (run-in / wash-out), 0a+b (screening phase), 1, 5, 9,
13, and 20. Descriptive statistics will be used to summarize continuous and categorical
variables. Mean change of Lp(a) levels will be compared between treatment and placebo group.
Subjects will be grouped according to treatment randomised (intention-to-treat, ITT
population). For missing data, the last observation will be carried forward (LOCF).
Comparisons between groups will be performed using analysis of covariance (ANCOVA) with
treatment as a factor, adjusting for baseline Lp(a) levels and other potential confounders.
Subgroup analyses will be performed according to Lp(a) phenotype, Lp(a) baseline level ( >
30-60 mg/dl, > 60 mg/dl), and concurrent statin therapy (yes / no).
Risks:
Flushing is the most common side effect of niacin. Other side effects include
gastrointestinal disorders (common) (diarrhoea, nausea, vomiting, abdominal pain, or
dyspepsia) and cardiac disorders (uncommon) (tachycardia, palpitations). A reversible
elevation of liver enzymes has been reported, as well as a decreased glucose tolerance,
reductions in platelet counts, increases in prothrombin time, elevations in uric acid
levels, and reductions in phosphorous levels (uncommon or rarely). Hypersensitivity
reactions have been reported very rarely.
Single reports on rhabdomyolysis in patients on combined therapy with niacin and HMG-CoA
reductase inhibitors (statins) have been reported. Careful monitoring for any signs and
symptoms of myopathy such as muscle pain, tenderness, or weakness is therefore required in
the case of combination therapy.
Benefit:
Niacin has been shown to improve the lipid profile in patients with reductions in total
cholesterol, LDL cholesterol and triglycerides and increases in HDL cholesterol. Niacin may
also reduce elevated Lp(a) levels and may thus lower cardiovascular events in the long term.
The following variables will be assessed prior randomisation: socio-demographic factors,
physical examinations, medical history, concurrent medication, health-related quality of
life, costs prior study entry, and lipid as well as other laboratory parameters. Lipid
parameters include Lp(a), total cholesterol, LDL cholesterol, HDL cholesterol, and
triglycerides.
At follow-up, the respective laboratory analyses and physical examinations will be assessed
at each visit. Subjects will be investigated with regard to safety and tolerability.
Health-related quality of life and costs will be assessed at week 9 and 20.
Eligibility
Minimum age: 18 Years.
Maximum age: 75 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Male or female subjects, aged 18 - 75 years
- Subjects with and without cardiovascular diseases
- Lp(a) plasma levels > 30 mg/dl
- Triglyceride levels < 400 mg/dl
- Cholesterol and triglyceride levels not requiring immediate change in medication
according to current clinical guidelines
- If concurrent statin therapy, stable doses are required in the four weeks prior study
inclusion, and no changes in statin dosages are allowed during the study period
- Subjects willing to follow all study procedures including attendance at practices for
scheduled study visits, fasting prior to blood draws and compliance with study
treatment regimen
- Written informed consent to participate in the trial
Exclusion Criteria:
- Known hypertriglyceridaemia or fasting triglycerides >= 400 mg/dl in the last four
weeks before the randomisation visit.
- Known heterozygous or homozygous familial hypercholesterolaemia or known type III
hyperlipoproteinaemia (familial dysbetalipoproteinaemia)
- Documented secondary hypercholesterolaemia of any cause
- Initiation of a lipid-modifying drug treatment or a dose change of a lipid-modifying
drug within the last four weeks
- Known hypersensitivity to nicotinic acid or any component of this medication or their
derivatives
- Concurrent treatment with products containing significant amounts (more than 100 mg
as daily dose) of nicotinic acid (niacin) or nicotinamide (e. g., vitamin preparations
and nutritional supplements)
- Concurrent treatment with an immediate release formulation of nicotinic acid or a
nicotinic acid analogue, e. g. supplements
- Treatment with an anticoagulant such as marcumar
- Cardiovascular diseases which are contra-indicated: unstable angina, acute myocardial
infarction or uncontrolled cardiac arrhythmias within the preceding 3 months, stroke
within the preceding 6 months, symptomatic heart failure (NYHA class III or IV), or
severe peripheral artery disease
- Pregnant women, women who are breast feeding, and women of childbearing potential who
are not using chemical or mechanical contraception (prescription oral contraceptives,
abstinence, condoms with spermicide, surgical sterilisation, diaphragm with
spermicide, or intrauterine device)
- History of malignancy, except subjects who have been disease free for more than 10
years or whose only malignancy has been basal or squamous cell skin carcinoma. Women
with a history of cervical dysplasia should be excluded unless 3 consecutive normal
cervical smears have subsequently been recorded before entry into the study.
- History of alcohol (more than 2 glasses of wine or alcohol equivalent per day) or
drug abuse (within 12 months of screening), or both
- Active liver disease or hepatic dysfunction as defined by elevations of AST or ALT
>=1. 5 times the ULN in the last 4 weeks before the randomisation visit
- Known uncontrolled or poorly controlled (HbA1C > 9 %) diabetes
- Persistent uncontrolled or untreated hypertension, defined as either resting
diastolic blood pressure of > 95 mmHg or resting systolic blood pressure of > 200
mmHg
- Unexplained serum creatine phosphokinase (CK) > 3 times the ULN in the last 4 weeks
before the randomisation visit (e. g. not due to recent trauma, intramuscular
injections, heavy exercise etc)
- History of severe myalgia of unknown origin
- Arterial bleeding
- Active peptic ulcer
- Uncontrolled endocrine or metabolic disease known to influence serum lipids or
lipoproteins
- Active gout symptoms
- Significant renal insufficiency (serum creatinine > 1. 5 mg/dl)
- Planned hospitalizations for diagnostic or surgical procedures within the next 5
months
- Known infectious disease such as hepatitis or HIV
- Participation in another investigational drug trial within the four weeks prior to
study entry
- Previous randomisation into this study
- Subjects with serious or unstable medical or psychological condition that, in the
opinion of the investigator, would compromise the subject's safety or successful
participation in the study.
- Persons who are detained officially or legally to an official institution.
Locations and Contacts
Institute of Social Medicine, Epidemiology and Health Economics, Berlin 10098, Germany
Additional Information
Starting date: January 2008
Last updated: August 3, 2009
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