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Advancing Niacin by Inhibiting Flushing (ANTI-FLUSH)

Phase 4
Completed
Conditions
Flushing
Interventions
Dietary Supplement: Quercetin
Dietary Supplement: Placebo
Registration Number
NCT00913081
Lead Sponsor
University of Pennsylvania
Brief Summary

Niacin, or vitamin B3, is known to improve cholesterol disorders and is the most effective drug to raise HDL, or the "good cholesterol". The use of niacin has been limited because of a peculiar adverse effect referred to as "flushing', which consists of redness, warmth, tingling and burning. A recent animal study suggests that flavonoids may prevent flushing due to niacin better than drugs like aspirin. The ANTI-FLUSH study is being done to assess whether a presently available dietary supplement known as quercetin, which is a flavonoid, can reduce the flushing that occurs with niacin. We will also assess whether using quercetin to prevent flushing from niacin, can improve how niacin lowers cholesterol.

Detailed Description

This study involves people between 21 and 75 years. It will be conducted over a period of 8 weeks, with 4 visits, each separated by 2 weeks. The duration of each visit is 9-10 hours. We will test a different dose of quercetin in each visit.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
17
Inclusion Criteria
  1. Men and women from the age of 21 to 75, inclusive - 16 subjects, 8 men, 8 women.
  2. Ability to understand and agree to informed consent.
  3. Are reliable and willing to make themselves available for the duration of the study and are willing to follow study procedures.
Exclusion Criteria
  1. Contra-indications or known intolerance to the study medications.
  2. History of congestive heart failure, carcinoid, rosacea, renal failure (GFR<60 ml/min/m2).
  3. Active liver disease.
  4. Active diabetes (defined as any history of type 1 diabetes, or history of type 2 diabetes plus one or more of the following: fasting glucose>= 126mg/dL at screening or use of anti-diabetic medications within 12 months, or glucose>200mg/dL 2 hours after a 75 g oral glucose challenge within 12 months.
  5. History of major surgery within the past 6 weeks, or anticipated major surgery during the course of the study, or any history of organ transplant.
  6. History of drug abuse within the past 3 years, or regular alcohol use of greater than 14 drinks per week.
  7. Women who are pregnant, plan to conceive or lactate.
  8. Peri-menopausal women or women currently experiencing flushing.
  9. Currently taking vasoactive medications, anti-hypertensives, anti-histamines, Selective Serotonin Re-uptake Inhibitors (SSRIs), NSAIDS, oral steroids, leukotriene inhibitors, supplemental quercetin and > 50mg niacin.

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Quercetin 500 mgQuercetinQuercetin 500 mg once, administered one hour before 500 mg immediate-release niacin
PlaceboPlaceboPlacebo once, administered one hour before 500 mg immediate-release niacin
Quercetin 2000 mgQuercetinQuercetin 2000 mg once, administered one hour before 500 mg immediate-release niacin
Quercetin 1000 mgQuercetinQuercetin 1000 mg once, administered one hour before 500 mg immediate-release niacin
Primary Outcome Measures
NameTimeMethod
Whether Quercetin Dose-dependently Reduces Laser Doppler Flux Index Primary Peak Following Immediate-release Niacin8 hour period

Laser Doppler flowmetry at the malar eminence measures blood flow quantitatively as red blood cell flux. Flux index is the fold-change in flux over baseline. Flux index primary peak is the maximum flux index between 0-4 hours after niacin.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (2)

CTRC Univ. of Penn - Andrew Mutch Bldg., 4th floor

🇺🇸

Phila, Pennsylvania, United States

University of Pennsylvania

🇺🇸

Phila, Pennsylvania, United States

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