CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 76 enrolled
Drug / intervention
Nebivolol +2 moredrug
Likely dose
Nebivolol 5 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01522950
NCT01522950Phase 2Completed

A Double-blind, Placebo-controlled, Randomized Study Examining the Effects of Nebivolol Compared to Atenolol on Endothelial Function and Cardiovascular Risk in Patients With Early Vascular Disease

University of Minnesota·interventional·Posted Feb 1, 2012·Updated Jul 17, 2020

In Brief

A Phase 2 clinical trial evaluating Nebivolol, atenolol, and 1 other intervention for Hypertension. Completed, enrolled 76 participants across 1 site.

Detailed Summary

This is a randomized, double-blind, placebo-controlled study comparing the efficacy of nebivolol and atenolol at improving small artery elasticity and reducing cardiovascular disease risk in subjects with early vascular disease. Approximately 75 subjects with borderline/elevated blood pressures and impaired endothelial function, as measured by arterial elasticity scores, will be recruited and assigned to treatment groups using a block randomization scheme. Patients will be randomly allocated to nebivolol, atenolol or placebo, and then followed for 9 months.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHypertension
CountriesUnited States
CollaboratorsForest Laboratories

Timeline

Phase 2CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedFeb 1, 2012
Enrollment StartMay 1, 2010
Primary CompletionOct 1, 2016
TodayJul 2, 2026
Enrollment to primary: 6.4 yearsPosted 14.4 years ago

Interventions

Nebivololdrug

5 mg daily or 10 mg daily

atenololdrug

25 mg daily or 50 mg daily

placebodrug

one tablet daily