Clinical Trials Directory

Trials / Completed

CompletedNCT01044693

Nebivolol in the Supine Hypertension of Autonomic Failure

Effect of Nebivolol on Blood Pressure in a Model of Hypertension Sensitive to Potentiation of Nitric Oxide Bioactivity

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Vanderbilt University · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the effect of the antihypertensive drug, nebivolol (Bystolic), compared to metoprolol (Lopressor) and sildenafil (Viagra) on blood pressure in patients with autonomic failure and supine hypertension.

Detailed description

Nebivolol is distinct among beta-blockers by its ability to increase nitric oxide (NO) bioactivity. The contribution of this effect to the pharmacological actions of the drug, however, is difficult to ascertain in normal subjects because of the confounding contribution of the autonomic nervous system. Autonomic failure patients provide a unique model of hypertension devoid of autonomic modulation but sensitive to NO mechanisms. We propose to determine the effect of nebivolol on blood pressure in this patient population. A decrease in blood pressure will imply increased bioactivity of NO. Comparisons will be made with placebo, metoprolol (as a negative control) and sildenafil (as a positive control).

Conditions

Interventions

TypeNameDescription
DRUGPlaceboPlacebo capsule
DRUGNebivolol 5 mgNebivolol 5mg single oral dose
DRUGmetoprolol tartrate 50 mgmetoprolol tartrate 50 mg single oral dose
DRUGSildenafil25 mgSildenafil 25 mg single oral dose

Timeline

Start date
2010-01-01
Primary completion
2014-07-01
Completion
2014-08-01
First posted
2010-01-08
Last updated
2015-05-01
Results posted
2015-05-01

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01044693. Inclusion in this directory is not an endorsement.