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An 8-week Multicenter, Randomized, Double-blind, Active Controlled, Parallel Group, Forced Titration Study to Evaluate the Efficacy and Safety of Aliskiren/Amlodipine/HCTZ Compared to Aliskiren/Amlodipine in US Minority Patients With Stage 2 Hypertension
The purpose of the study is to compare the combination of aliskiren, amlodipine and Hydrochlorothiazide (HCTZ) versus the combination of aliskiren and amlodipine as therapy in minority Stage 2 hypertensive patients.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
K and S Research Services
Little Rock, Arkansas, United States
Well Pharma Medical Research
South Miami, Florida, United States
Hyde Park Health Associates
Mattapan, Massachusetts, United States
Manassas Clinical Research Center
Manassas, Virginia, United States
Scriber Kidney Center
Seattle, Washington, United States
Start Date
June 1, 2009
Primary Completion Date
March 1, 2010
Last Updated
June 8, 2011
412
ACTUAL participants
Aliskiren/Amlodipine
DRUG
Aliskiren/Amlodipine and Hydrochlorothiazide (HCTZ)
DRUG
Lead Sponsor
Novartis
NCT02417740
NCT07073820
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07480265