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Completed Phase 4 Interventional Results available

8-week Randomized, Open-label Study to Evaluate Food Effect on Efficacy and Safety of Oral Aliskiren 300 mg in Patients With Hypertension

ClinicalTrials.gov ID: NCT01570686

Public ClinicalTrials.gov record NCT01570686. 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 May 16, 2026, 6:39 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

An 8-week Randomized, Open-label, Multi-center Study to Evaluate the Efficacy and Safety of Oral Aliskiren 300 mg Once Daily Under Light Meal Versus Fasted Condition in Patients With Hypertension

Study identification

NCT ID
NCT01570686
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
589 participants

Conditions and interventions

Conditions

Interventions

  • Aliskiren 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
Mar 31, 2012
Primary completion
Oct 31, 2012
Completion
Oct 31, 2012
Last update posted
Jan 21, 2014

2012

United States locations

U.S. sites
43
U.S. states
18
U.S. cities
41
Facility City State ZIP Site status
Novartis Investigative Site Los Angeles California 90057
Novartis Investigative Site Riverside California 92506
Novartis Investigative Site Santa Monica California 90404
Novartis Investigative Site Walnut Creek California 94598
Novartis Investigative Site Westlake Village California 91361
Novartis Investigative Site Coral Gables Florida 33134
Novartis Investigative Site Miami Florida 33169
Novartis Investigative Site South Miami Florida 33143
Novartis Investigative Site Chicago Illinois 60607
Novartis Investigative Site Chicago Illinois 60610
Novartis Investigative Site Evansville Indiana 47712
Novartis Investigative Site Topeka Kansas 66606
Novartis Investigative Site Opelousas Louisiana 70570
Novartis Investigative Site Chaska Minnesota 55318
Novartis Investigative Site Edina Minnesota 55435
Novartis Investigative Site Saint Paul Minnesota 55114
Novartis Investigative Site Jackson Mississippi 39209
Novartis Investigative Site Picayune Mississippi 39466
Novartis Investigative Site St Louis Missouri 63141
Novartis Investigative Site Charlotte North Carolina 28209
Novartis Investigative Site Greensboro North Carolina 27401
Novartis Investigative Site Greensboro North Carolina 27408
Novartis Investigative Site Salisbury North Carolina 28144
Novartis Investigative Site Shelby North Carolina 28152
Novartis Investigative Site Winston-Salem North Carolina 27103
Novartis Investigative Site Cincinnati Ohio 45246
Novartis Investigative Site Columbus Ohio 43213
Novartis Investigative Site Lyndhurst Ohio 44124
Novartis Investigative Site Marion Ohio 43302
Novartis Investigative Site Norman Oklahoma 73069
Novartis Investigative Site Eugene Oregon 97404
Novartis Investigative Site Oregon City Oregon 97045
Novartis Investigative Site Portland Oregon 97239
Novartis Investigative Site Knoxville Tennessee 37920
Novartis Investigative Site Beaumont Texas 77702
Novartis Investigative Site Houston Texas 77081
Novartis Investigative Site Lake Jackson Texas 77566
Novartis Investigative Site Pasadena Texas 77504
Novartis Investigative Site Centerville Utah 84104
Novartis Investigative Site Arlington Virginia 22203
Novartis Investigative Site Ettrick Virginia 23803
Novartis Investigative Site Midlothian Virginia 23114
Novartis Investigative Site Port Orchard Washington 98366

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 40 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01570686, 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 Jan 21, 2014 · Synced May 16, 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 protocol, eligibility criteria, and contact information for NCT01570686 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →