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NCT00200434 · ClinicalTrials.gov registry record · Phase 3

A Study of the Efficacy and Safety of Nebivolol Added to Existing Antihypertensive Treatment in Patients With Hypertension

A Phase 3 study, sponsored by Mylan Bertek Pharmaceuticals.

Completed
Registry status
Phase 3
Development phase
600
Enrollment target

NCT00200434: Completed Phase 3 study, sponsored by Mylan Bertek Pharmaceuticals.

NCT00200434 is a Phase 3 study that has completed, run by Mylan Bertek Pharmaceuticals. The registered enrollment target is 600 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00200434, a Phase 3 study, has completed, sponsored by Mylan Bertek Pharmaceuticals.

COMPLETED
Registry status
Phase 3
Development phase
600 participants
Enrollment target

Study Summary

The purpose of this study was to contrast the efficacy and safety of 3 dose levels of nebivolol vs. placebo, when added to a patient's existing antihypertensive medication(s) for 3 months, in patients with mild to moderate hypertension

Interventions

  • DRUG Nebivolol

Trial Details

FieldValue
Enrollment Target 600 participants
Start Date 2002-10
Est. Completion 2003-10
Phase Phase 3

Sponsor

Mylan Bertek Pharmaceuticals

10 total trials

What the Registry Record Tells You About NCT00200434

The ClinicalTrials.gov registry entry for NCT00200434 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 600 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Mylan Bertek Pharmaceuticals, which has 10 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Nebivolol is the first listed.

NCT00200434 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00200434 about?

NCT00200434 is a clinical study titled "A Study of the Efficacy and Safety of Nebivolol Added to Existing Antihypertensive Treatment in Patients With Hypertension". The purpose of this study was to contrast the efficacy and safety of 3 dose levels of nebivolol vs. placebo, when added to a patient's existing antihypertensive medication(s) for 3 months, in patients with mild to moderate hypertension

What is the current status of trial NCT00200434?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 600 participants. The study started on 2002-10. Estimated completion is 2003-10.

What interventions are being tested in trial NCT00200434?

The interventions under investigation include: Nebivolol (DRUG).

Who is sponsoring clinical trial NCT00200434?

This trial is sponsored by Mylan Bertek Pharmaceuticals, which has 10 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.