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Completed Phase 4 Interventional Results available

A Study on the Long-term Efficacy of Nebivolol After Withdrawal of Therapy

ClinicalTrials.gov ID: NCT00785512

Public ClinicalTrials.gov record NCT00785512. 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 Jul 22, 2026, 8:43 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

A Prospective, Randomized, Double-Blind, Placebo Controlled Study of the Long-Term Efficacy of Nebivolol in Hypertensive Patients After Withdrawal of Therapy

Study identification

NCT ID
NCT00785512
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Forest Laboratories
Industry
Enrollment
207 participants

Conditions and interventions

Conditions

Interventions

  • Nebivolol Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 79 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 31, 2008
Primary completion
Jul 31, 2009
Completion
Not listed
Last update posted
Sep 14, 2010

Started 2008

United States locations

U.S. sites
26
U.S. states
10
U.S. cities
23
Facility City State ZIP Site status
Forest Investigative Site Chandler Arizona 85225
Forest Investigative Site Phoenix Arizona 85050
Forest Investigative Site Los Angeles California 90057
Forest Investigative Site Bradenton Florida 34203
Forest Investigative Site Brooksville Florida 34613
Forest Investigative Site DeLand Florida 32720
Forest Investigative Site Hollywood Florida 33021
Forest Investigative Site Miami Florida 33014
Forest Investigative Site Miami Florida 33156
Forest Investigative Site Miami Florida 33169
Forest Investigative Site Pembroke Pines Florida 33024
Forest Investigative Site St. Petersburg Florida 33709
Forest Investigative Site Auburn Maine 04210
Forest Investigative Site Cary North Carolina 27518
Forest Investigative Site Hickory North Carolina 28601
Forest Investigative Site Salisbury North Carolina 28144
Forest Investigative Site Wilmington North Carolina 28401
Forest Investigative Site Winston-Salem North Carolina 27103
Forest Investigative Site Cincinnati Ohio 45242
Forest Investigative Site Marion Ohio 43302
Forest Investigative Site Lancaster Pennsylvania 17601
Forest Investigative Site Mt. Pleasant South Carolina 29464
Forest Investigative Site Simpsonville South Carolina 29681
Forest Investigative Site New Tazewell Tennessee 37825
Forest Investigative Site Dallas Texas 75231
Forest Investigative Site Dallas Texas 75234

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 NCT00785512, 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 Sep 14, 2010 · Synced Jul 22, 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 NCT00785512 live on ClinicalTrials.gov.

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