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Completed Phase 3 Interventional

A Study To Evaluate the Effect of Rosuvastatin On Intravascular Ultrasound-Derived Coronary Atheroma Burden (ASTEROID)

ClinicalTrials.gov ID: NCT00240318

Public ClinicalTrials.gov record NCT00240318. 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, 2:23 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

A 104-Week, Open-label, Multi-centre, Phase IIIb Study Evaluating the Effect of Treatment With Rosuvastatin 40 mg on Atherosclerotic Disease as Measured by Intravascular Ultrasound and Quantitative Coronary Angiography in Subjects Undergoing Coronary Angiography Who Have Coronary Artery Disease

Study identification

NCT ID
NCT00240318
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
450 participants

Conditions and interventions

Interventions

  • Rosuvastatin calcium 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
Oct 31, 2002
Primary completion
Oct 31, 2005
Completion
Oct 31, 2005
Last update posted
Nov 18, 2010

2002 – 2005

United States locations

U.S. sites
24
U.S. states
16
U.S. cities
24
Facility City State ZIP Site status
Research Site Birmingham Alabama
Research Site Los Angeles California
Research Site San Francisco California
Research Site Santa Rosa California
Research Site Stockton California
Research Site Denver Colorado
Research Site Hartford Connecticut
Research Site Atlantis Florida
Research Site Chicago Illinois
Research Site Maywood Illinois
Research Site Auburn Maine
Research Site Baltimore Maryland
Research Site Ann Arbor Michigan
Research Site Petoskey Michigan
Research Site Minneapolis Minnesota
Research Site Saint Paul Minnesota
Research Site Buffalo New York
Research Site Valhalla New York
Research Site Williamsville New York
Research Site Chapel Hill North Carolina
Research Site Toledo Ohio
Research Site Danville Pennsylvania
Research Site Houston Texas
Research Site Milwaukee Wisconsin

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 37 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00240318, 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 Nov 18, 2010 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00240318 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →