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Completed Phase 3 Interventional Results available

Study to Evaluate the EFFECTS of Acetylsalicylic Acid (ASA) on Niaspan®-Induced Flushing in Subjects With Dyslipidemia

ClinicalTrials.gov ID: NCT00626392

Public ClinicalTrials.gov record NCT00626392. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 4:20 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Multicenter, Randomized, Double-Blind, Parallel, Acetylsalicylic Acid (ASA) Run-In Study to Evaluate the EFFECTS of Acetylsalicylic Acid on Niaspan®-Induced Flushing in Subjects With Dyslipidemia

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary purpose of this study was to assess the effect of aspirin (ASA) on niacin extended-release (NER)-induced flushing in subjects with dyslipidemia.

Study identification

NCT ID
NCT00626392
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Abbott
Industry
Enrollment
277 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 2008 (Type not available)
Primary completion
Apr 2008 (Actual)
Completion
Apr 2008 (Actual)
Last update posted
Sep 2, 2009

2008

United States locations

U.S. sites
26
U.S. states
11
U.S. cities
25
Facility City State ZIP Site status
Not listed Huntsville Alabama 35801 —
Not listed Scottsdale Arizona 85251 —
Not listed Tucson Arizona 85710 —
Not listed Tucson Arizona 85712 —
Not listed Anaheim California 92801 —
Not listed Los Angeles California 90057 —
Not listed Newport Beach California 92660 —
Not listed Stockton California 95204 —
Not listed Vista California 90057 —
Not listed Westlake Village California 91361 —
Not listed Coral Gables Florida 33134 —
Not listed Jacksonville Florida 32259 —
Not listed Miami Florida 33186 —
Not listed Pembroke Pines Florida 33027 —
Not listed West Palm Beach Florida 33407 —
Not listed North Dartmouth Massachusetts 02747 —
Not listed Rochester New York 14609 —
Not listed Charlotte North Carolina 28262 —
Not listed Winston-Salem North Carolina 27103 —
Not listed Penndel Pennsylvania 19047 —
Not listed Johnston Rhode Island 02919 —
Not listed Mt. Pleasant South Carolina 29464 —
Not listed Simpsonville South Carolina 29681 —
Not listed Colleyville Texas 76034 —
Not listed Houston Texas 77074 —
Not listed San Antonio Texas 78229 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00626392, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 2, 2009 · Synced Oct 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00626392 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →