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A 6-Week Multi-center, Randomized, Double-Blind, Parallel Group Study Comparing the Efficacy of Amlodipine Besylate/Benazepril Versus Amlodipine in the Treatment of Severe Hypertension
This trial is designed to study the efficacy of an amlodipine besylate/benazepril treatment regimen versus an amlodipine treatment regimen in the treatment of severe hypertension.
Age
18 - 80 years
Sex
ALL
Healthy Volunteers
No
Novartis Pharmaceuticals
East Hanover, New Jersey, United States
Start Date
December 1, 2004
Primary Completion Date
July 1, 2005
Completion Date
July 1, 2005
Last Updated
November 8, 2011
259
ACTUAL participants
amlodipine besylate/benazepril hydrochloride
DRUG
Lead Sponsor
Novartis Pharmaceuticals
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