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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 Jul 22, 2026, 10:49 AM 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

Study identification

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

Conditions and interventions

Conditions

Interventions

  • niacin extended-release (NER) Drug
  • aspirin (ASA) Drug
  • aspirin placebo (ASA Pbo) Drug

Drug

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
Jan 31, 2008
Primary completion
Mar 31, 2008
Completion
Mar 31, 2008
Last update posted
Sep 1, 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 1, 2009 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00626392 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →