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Blood Pressure and Metabolic Effects of Nebivolol Compared With Hydrochlorothiazide and Placebo in Hypertensive Patients With Impaired Glucose Tolerance or Impaired Fasting Glucose
This study is being done to see if the blood pressure and metabolic effects of an approved drug nebivolol is comparable to that of another approved drug hydrochlorothiazide (HCTZ) and placebo in hypertensive patients.
This study is double blind (neither you nor the physician will know when you are receiving placebo, which is an inactive compound such as a sugar pill, or active study drugs nebivolol or hydrochlorothiazide). All participants will also receive lisinopril, an angiotensin converting enzyme, or losartan, an angiotensin receptor blocker. All medications are approved and marketed for the treatment of hypertension.This study is being conducted in about 500 patients at approximately 80 research centers in the United States. The study consists of approximately 9 study visits over a period of 5 months. During these visits, patients will undergo routine health exams and some special laboratory tests such as an oral glucose tolerance test.
Age
18 - 80 years
Sex
ALL
Healthy Volunteers
No
Forest Investigative Site 058
Athens, Alabama, United States
Forest Investigative Site 101
Birmingham, Alabama, United States
Forest Investigative Site 016
Huntsville, Alabama, United States
Forest Investigative Site 119
Phoenix, Arizona, United States
Forest Investigative Site 078
Tucson, Arizona, United States
Forest Investigative Site 056
Anaheim, California, United States
Forest Investigative Site 097
Bell Gardens, California, United States
Forest Investigative Site 026
Buena Park, California, United States
Forest Investigative Site 147
Buena Park, California, United States
Forest Investigative Site 061
Chino, California, United States
Start Date
May 15, 2008
Primary Completion Date
July 9, 2010
Completion Date
July 9, 2010
Last Updated
February 26, 2020
537
ACTUAL participants
Nebivolol with concomitant losartan or lisinopril
DRUG
HCTZ with concomitant losartan or lisinopril
DRUG
Placebo with concomitant losartan or lisinopril
DRUG
Lead Sponsor
Forest Laboratories
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.
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