Novel Pathways to Manage Inflammation and Atherosclerosis in Dialysis Patients: Role of Nicotinic Acid
This study is ongoing, but not recruiting participants.
Sponsor:
Brigham and Women's Hospital
Information provided by (Responsible Party):
Kambiz Zandi-Nejad, MD, Brigham and Women's Hospital
ClinicalTrials.gov Identifier:
NCT01159054
First received: July 7, 2010
Last updated: May 22, 2012
Last verified: May 2012
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Purpose
Patients with kidney failure on hemodialysis have an extremely high rate of cardiovascular disease including atherosclerotic cardiovascular disease. This, at least in part, is due to the chronic inflammatory status usually seen in these patients. Here we try to see if treatment with extended release nicotinic acid (Niaspan) can reduce their overall inflammatory burden (in general) and the atherosclerotic plaque inflammation (in particular).
| Condition | Intervention |
|---|---|
|
Dialysis Cardiovascular Disease Atherosclerosis Inflammation |
Drug: Extended Release Nicotinic Acid (Niaspan) |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Novel Pathways to Manage Inflammation and Atherosclerosis in Dialysis Patients: Role of Nicotinic Acid |
Resource links provided by NLM:
Further study details as provided by Brigham and Women's Hospital:
Primary Outcome Measures:
- Changes in FDG-PET/CT dual scan score [ Time Frame: 6 months ] [ Designated as safety issue: No ]
- Changes in hs-CRP level [ Time Frame: 6 monhts ] [ Designated as safety issue: No ]
- Changes in IL-6 level [ Time Frame: 6 months ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Albumin level [ Time Frame: 6 months ] [ Designated as safety issue: No ]
- ESA dose requirement [ Time Frame: 6 months ] [ Designated as safety issue: No ]
- Hemoglobin level [ Time Frame: 6 months ] [ Designated as safety issue: No ]
- Rate of cardiovascular events [ Time Frame: 6 months ] [ Designated as safety issue: No ]
- Hemodialysis access stenosis/thrombosis [ Time Frame: 6 months ] [ Designated as safety issue: No ]
- Incidence of rises in liver function tests [ Time Frame: 6 months (checked monthly) ] [ Designated as safety issue: Yes ]
| Estimated Enrollment: | 32 |
| Study Start Date: | July 2010 |
| Estimated Study Completion Date: | June 2013 |
| Estimated Primary Completion Date: | June 2013 (Final data collection date for primary outcome measure) |
Intervention Details:
-
Drug: Extended Release Nicotinic Acid (Niaspan)
- Extended Release Nicotinic Acid
- Niaspan
Subjects will start on 500 mg per day of Niaspan for 4 weeks, then the dose will be increased to 1000 mg per day of Niaspan for 4 weeks, then the dose will be increased to 1500 mg of Niaspan per day for 4 weeks, after this subjects with weight of less than 60 kg will continue at 1500 mg per day of Niaspan for another 12 weeks whereas in subjects with weight of more than 60 kg the dose will be increased to 2000 mg of Niaspan per day which will be continued for 12 weeks.
Other Names:
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- A signed consent form;
- Male or Female, 18 years or older;
- Diagnosed with ESRD, on maintenance hemodialysis for at least six (6) months;
- Subject must be able to understand and provide informed consent;
- No known contraindications to therapy with nicotinic acid;
- Female subjects of childbearing potential must be willing to be on an acceptable form of birth control for the duration of the study and for two month after they have stopped taking the study drug.
Exclusion Criteria:
- Any patient with a medical condition or taking any medications that would be contraindicated with the use of extended release niacin, such as active peptic ulcer disease;
- History of severe allergic reactions to the study medication;
- History of active infection or acute gouty attack within 2 weeks prior to enrollment;
- Known serological positivity for HIV, HBsAg, or HCV Ab;
- HbA1C > 9;
- Total CK of more than three times of the upper limit of normal;
- Elevation of liver function tests at time of entry (AST and/or ALT > 2 times the upper limit of normal);
- History of drug, alcohol, or chemical abuse within 6 months prior to enrollment;
- History of malignancy except adequately treated in-situ cervical carcinoma, or adequately treated basal or squamous cell carcinoma of the skin;
- History of an inflammatory disease such as SLE, rheumatoid arthritis or ulcerative colitis;
- Patients currently on pharmacological doses of nicotinic acid;
- Patients receiving chronic anti-inflammatory therapy;
- Patients with average baseline hs-CRP levels of > 20 mg/L or < 1 mg/L;
- Patients in whom FDG-PET/CT dual scans are contraindicated (e.g., pregnant patients or those with severe allergy to IV contrast; a pregnancy test will be performed in each female subject between 18 and 45 years of age prior to each scan)
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01159054
Locations
| United States, Massachusetts | |
| Brigham and Women's Hospital | |
| Boston, Massachusetts, United States, 02115 | |
| BWH/FH/DCI Outpatient Dialysis Unit | |
| Boston, Massachusetts, United States, 02130 | |
| DCI Dialysis Unit-Somerville | |
| Somerville, Massachusetts, United States | |
Sponsors and Collaborators
Brigham and Women's Hospital
Investigators
| Principal Investigator: | Kambiz ZANDI-NEJAD, MD | Brigham and Women's Hospital |
More Information
No publications provided
| Responsible Party: | Kambiz Zandi-Nejad, MD, Instructor in Medicine, Brigham and Women's Hospital |
| ClinicalTrials.gov Identifier: | NCT01159054 History of Changes |
| Other Study ID Numbers: | 2010P001049 |
| Study First Received: | July 7, 2010 |
| Last Updated: | May 22, 2012 |
| Health Authority: | United States: Institutional Review Board |
Additional relevant MeSH terms:
|
Atherosclerosis Cardiovascular Diseases Inflammation Arteriosclerosis Arterial Occlusive Diseases Vascular Diseases Pathologic Processes Nicotinic Acids Niacin Niacinamide Vitamin B Complex Vitamins |
Micronutrients Growth Substances Physiological Effects of Drugs Pharmacologic Actions Vasodilator Agents Cardiovascular Agents Therapeutic Uses Hypolipidemic Agents Antimetabolites Molecular Mechanisms of Pharmacological Action Lipid Regulating Agents |
ClinicalTrials.gov processed this record on May 16, 2013