Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Efficacy and Safety of Aliskiren and Aliskiren/Enalapril Combination on Morbidity-mortality in Patients With Chronic Heart Failure

ClinicalTrials.gov ID: NCT00853658

Public ClinicalTrials.gov record NCT00853658. 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 20, 2026, 10:27 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 Multicenter, Randomized, Double-blind, Parallel Group, Active-controlled Study to Evaluate the Efficacy and Safety of Both Aliskiren Monotherapy and Aliskiren/Enalapril Combination Therapy Compared to Enalapril Monotherapy, on Morbidity and Mortality in Patients With Chronic Heart Failure (NYHA Class II - IV). The Study is Also Known as Aliskiren Trial of Minimizing OutcomeS in Patients With HEart Failure (ATMOSPHERE).

Brief summary

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

The study will evaluate the efficacy and safety of both aliskiren monotherapy and aliskiren/enalapril combination therapy as compared to enalapril monotherapy, on morbidity and mortality in patients with chronic heart failure (NYHA Class II - IV.

Study identification

NCT ID
NCT00853658
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
7,064 participants

Conditions and interventions

Interventions

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
Mar 2009 (Type not available)
Primary completion
Oct 2015 (Actual)
Completion
Oct 2015 (Actual)
Last update posted
Nov 25, 2016

2009 – 2015

United States locations

U.S. sites
58
U.S. states
22
U.S. cities
54
Facility City State ZIP Site status
Novartis Investigative Site Huntsville Alabama 35801 —
Novartis Investigative Site Mobile Alabama 36608 —
Novartis Investigative Site Mobile Alabama 36693 —
Novartis Investigative Site Tucson Arizona 85723-0001 —
Novartis Investigative Site Hot Springs Arkansas 71913 —
Novartis Investigative Site Little Rock Arkansas 72204 —
Novartis Investigative Site Little Rock Arkansas 72205 —
Novartis Investigative Site Pine Bluff Arkansas 71603 —
Novartis Investigative Site Searcy Arkansas 72143 —
Novartis Investigative Site Beverly Hills California 90211 —
Novartis Investigative Site French Camp California 95231 —
Novartis Investigative Site Inglewood California 90301 —
Novartis Investigative Site Los Angeles California 90073 —
Novartis Investigative Site Modesto California 95355 —
Novartis Investigative Site Northridge California 91325 —
Novartis Investigative Site Sacramento California 95825 —
Novartis Investigative Site San Diego California 92123 —
Novartis Investigative Site Santa Monica California 90404 —
Novartis Investigative Site Westlake Village California 91361 —
Novartis Investigative Site Denver Colorado 80218 —
Novartis Investigative Site Littleton Colorado 80120 —
Novartis Investigative Site Boynton Beach Florida 33437 —
Novartis Investigative Site Daytona Beach Florida 32117 —
Novartis Investigative Site Fort Lauderdale Florida 33316 —
Novartis Investigative Site Hollywood Florida 33021 —
Novartis Investigative Site Jacksonville Beach Florida 32050 —
Novartis Investigative Site Miami Lakes Florida 33014 —
Novartis Investigative Site Orlando Florida 32803 —
Novartis Investigative Site Wellington Florida 33449 —
Novartis Investigative Site Athens Georgia 30606 —
Novartis Investigative Site Augusta Georgia 30904 —
Novartis Investigative Site Gillespie Illinois 62033 —
Novartis Investigative Site Topeka Kansas 66606 —
Novartis Investigative Site Metairie Louisiana 70006 —
Novartis Investigative Site New Orleans Louisiana 70121 —
Novartis Investigative Site Slidell Louisiana 70458 —
Novartis Investigative Site Auburn Maine 04210 —
Novartis Investigative Site Southfield Michigan 48075 —
Novartis Investigative Site St Louis Missouri 63110 —
Novartis Investigative Site Lincoln Nebraska 68506 —
Novartis Investigative Site Omaha Nebraska 68198 —
Novartis Investigative Site Elmer New Jersey 08318 —
Novartis Investigative Site Laurelton New York 11422 —
Novartis Investigative Site Stony Brook New York 11794 —
Novartis Investigative Site Wiliamsville New York 14221 —
Novartis Investigative Site Durham North Carolina 27710 —
Novartis Investigative Site Marion Ohio 43302 —
Novartis Investigative Site Charleston South Carolina 29403 —
Novartis Investigative Site Varnville South Carolina 29944 —
Novartis Investigative Site Germantown Tennessee 38138 —
Novartis Investigative Site Memphis Tennessee 38120 —
Novartis Investigative Site Nashville Tennessee 37205 —
Novartis Investigative Site Nashville Tennessee 37212 —
Novartis Investigative Site Dallas Texas 75226 —
Novartis Investigative Site Houston Texas 77021 —
Novartis Investigative Site Houston Texas 77030 —
Novartis Investigative Site Everett Washington 98208 —
Novartis Investigative Site Kirkland Washington 98034 —

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 748 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00853658, 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 25, 2016 · Synced Oct 20, 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 NCT00853658 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →