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Completed Phase 3 Interventional Results available

Safety and Efficacy of Aliskiren on the Progression of Atherosclerosis in Coronary Artery Disease Patients

ClinicalTrials.gov ID: NCT00853827

Public ClinicalTrials.gov record NCT00853827. 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 25, 2026, 4:37 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

A 104 Week, Randomized, Double Blind, Placebo-controlled, Parallel-group, Multicenter Study to Evaluate the Efficacy of Aliskiren on the Progression of Atherosclerosis in Patients With Coronary Artery Disease When Added to Optimal Background Therapy

Brief summary

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

The study will assess the change in coronary atherosclerotic disease as determined by intravascular ultrasound (IVUS) for aliskiren compared to placebo when given in addition to standard therapy in patients with coronary artery disease (CAD) and a blood pressure in the pre-hypertensive range.

Study identification

NCT ID
NCT00853827
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
613 participants

Conditions and interventions

Eligibility (public fields only)

Age range
35 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
Mar 2009 (Type not available)
Primary completion
Jan 2013 (Actual)
Completion
Jan 2013 (Actual)
Last update posted
Jun 3, 2014

2009 – 2013

United States locations

U.S. sites
54
U.S. states
27
U.S. cities
51
Facility City State ZIP Site status
Novartis Investigative Site Mobile Alabama 36693 —
Novartis Investigative Site Phoenix Arizona 85054 —
Novartis Investigative Site Tucson Arizona 85723-0001 —
Novartis Investigative Site Tucson Arizona 85745 —
Novartis Investigative Site Los Angeles California 90033 —
Novartis Investigative Site Los Angeles California 90095 —
Novartis Investigative Site San Diego California 92161 —
Novartis Investigative Site Stockton California 95204 —
Novartis Investigative Site Torrance California 90502 —
Novartis Investigative Site Boulder Colorado 80304 —
Novartis Investigative Site Farmington Connecticut 06030-3100 —
Novartis Investigative Site Washington D.C. District of Columbia 20010 —
Novartis Investigative Site Washington D.C. District of Columbia 20037 —
Novartis Investigative Site Gainesville Florida 32610 —
Novartis Investigative Site Hudson Florida 34667 —
Novartis Investigative Site Miami Florida 33137-3732 —
Novartis Investigative Site Port Charlotte Florida 33952 —
Novartis Investigative Site Safety Harbor Florida 34695 —
Novartis Investigative Site Decatur Georgia 30033 —
Novartis Investigative Site Elkhart Indiana 46514 —
Novartis Investigative Site Lexington Kentucky 40536 —
Novartis Investigative Site Louisville Kentucky 40202 —
Novartis Investigative Site Covington Louisiana 70433 —
Novartis Investigative Site Columbia Maryland 21044 —
Novartis Investigative Site Boston Massachusetts — —
Novartis Investigative Site Flint Michigan 48532 —
Novartis Investigative Site Kalamazoo Michigan 49048 —
Novartis Investigative Site Midland Michigan 48640 —
Novartis Investigative Site Petoskey Michigan 49770 —
Novartis Investigative Site Saginaw Michigan 48601 —
Novartis Investigative Site Rochester Minnesota 55905-0001 —
Novartis Investigative Site Saint Paul Minnesota 55102 —
Novartis Investigative Site Columbia Missouri 65212 —
Novartis Investigative Site Ridgewood New Jersey 07450 —
Novartis Investigative Site Albuquerque New Mexico 87131-5271 —
Novartis Investigative Site Buffalo New York 14215 —
Novartis Investigative Site New York New York 10011 —
Novartis Investigative Site Syracuse New York 13210-1640 —
Novartis Investigative Site Williamsville New York 14221 —
Novartis Investigative Site Raleigh North Carolina 27610 —
Novartis Investigative Site Fargo North Dakota 58122 —
Novartis Investigative Site Cleveland Ohio 44109-1998 —
Novartis Investigative Site Oklahoma City Oklahoma 73109 —
Novartis Investigative Site Tulsa Oklahoma 74104-4243 —
Novartis Investigative Site Bend Oregon 97701 —
Novartis Investigative Site Hillsboro Oregon 97123 —
Novartis Investigative Site Danville Pennsylvania 17822-2001 —
Novartis Investigative Site Pittsburgh Pennsylvania 15213 —
Novartis Investigative Site Johnson City Tennessee 37604 —
Novartis Investigative Site Memphis Tennessee 38104 —
Novartis Investigative Site Oak Ridge Tennessee 37830 —
Novartis Investigative Site Dallas Texas 75226 —
Novartis Investigative Site Katy Texas 77493 —
Novartis Investigative Site San Antonio Texas 78229-3900 —

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 75 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00853827, 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 Jun 3, 2014 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00853827 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →