ClinicalTrials.Veeva

Menu

Novel Pathways to Manage Inflammation and Atherosclerosis in Dialysis Patients: Role of Nicotinic Acid

Mass General Brigham logo

Mass General Brigham

Status

Terminated

Conditions

Inflammation
Dialysis
Atherosclerosis
Cardiovascular Disease

Treatments

Drug: Extended Release Nicotinic Acid (Niaspan)

Study type

Interventional

Funder types

Other

Identifiers

NCT01159054
2010P001049

Details and patient eligibility

About

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).

Enrollment

22 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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)

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

22 participants in 1 patient group

This study has only one arm.
Experimental group
Description:
Blood sample and scan results to be compared before and after intervention in each subject.
Treatment:
Drug: Extended Release Nicotinic Acid (Niaspan)

Trial contacts and locations

3

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems