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Terminated Phase 3 Interventional Results available

Study to Evaluate Symptoms in Patients Treated With Nebivolol or Metoprolol Extended-release (ER) for Hypertension

ClinicalTrials.gov ID: NCT00547300

Public ClinicalTrials.gov record NCT00547300. 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 5, 2026, 6:50 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

Tolerability of Nebivolol Compared With Metoprolol ER in Patients With Mild to Moderate Hypertension Taking Hydrochlorothiazide (HCTZ)

Study identification

NCT ID
NCT00547300
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Forest Laboratories
Industry
Enrollment
49 participants

Conditions and interventions

Conditions

Interventions

  • Metoprolol ER Drug
  • Nebivolol Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 80 Years
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
Oct 30, 2007
Primary completion
Jan 1, 2008
Completion
Jan 1, 2008
Last update posted
May 20, 2019

2007 – 2008

United States locations

U.S. sites
24
U.S. states
11
U.S. cities
24
Facility City State ZIP Site status
Forest Research Institute 014 Birmingham Alabama 35205
Forest Research Institute 028 Beverly Hills California 90211
Forest Research Institute 054 Encinitas California 92024
Forest Research Institute 025 Roseville California 95661
Forest Research Institute 013 Tustin California 92780
Forest Research Institute 053 Vista California 92083
Forest Research Institute 052 Walnut Creek California 94598
Forest Research Institute 033 Westlake Village California 91361
Forest Research Institute 010 DeLand Florida 32720
Forest Research Institute 019 Holly Hill Florida 32117
Forest Research Institute 036 Hollywood Florida 33023
Forest Research Institute 007 Pembroke Pines Florida 33024
Forest Research Institute 009 Atlanta Georgia 30338
Forest Research Institute 006 Oxon Hill Maryland 20745
Forest Research Institute 027 Las Vegas Nevada 89106
Forest Research Institute 050 Salisbury North Carolina 28144
Forest Research Institute 039 Wilmington North Carolina 28401
Forest Investigative Site 002 Charleston South Carolina 29407
Forest Research Institute 032 Greenville South Carolina 29615
Forest Research Institute 008 Nashville Tennessee 37203
Forest Research Institute 003 Carrollton Texas 75006
Forest Research Institute 012 San Antonio Texas 78229
Forest Research Institute 048 Sugar Land Texas 77479
Forest Research Institute 040 Bountiful Utah 84010

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00547300, 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 May 20, 2019 · Synced May 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00547300 live on ClinicalTrials.gov.

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