Key result
This paper is a study protocol for a randomized controlled trial comparing nebivolol and carvedilol in older patients with heart failure and preserved ejection fraction, and contains no results.
Why the study?
Does nebivolol improve left ventricular diastolic function more than carvedilol in older patients with heart failure with preserved ejection fraction?
RCT (n=62)
Open-label
1:1
No
Does nebivolol improve left ventricular diastolic function more than carvedilol in older patients with heart failure with preserved ejection fraction?
This study protocol outlines a randomized trial to compare the effects of nebivolol versus carvedilol on left ventricular diastolic function in older patients with HFpEF.
BACKGROUND: Heart failure (HF) is a common and disabling condition in older people. Randomized clinical trials and meta-analyses have clearly demonstrated that the long-term use of β-Blockers improves the outcome of patients with HF. However, limited data are available on the treatment of older HF patients with preserved ejection fraction (EF). No study has specifically compared the relative effectiveness of carvedilol and nebivolol in treating HF in older patients with preserved EF. METHOD/DESIGN: This trial is a prospective, randomized, open-label, single-centre, active controlled study designed to investigate the effects of nebivolol and carvedilol on diastolic function of the left ventricle (LV) in older HF patients with preserved EF. We will test the hypothesis that nebivolol improves LV diastolic function to a greater extent than carvedilol in patients over 70 years of age. The study population includes 62 older patients newly diagnosed with HF. Patients will be included in the study if they have a LVEF ≥40 %, New York Heart Association (NYHA) functional classes I, II or III status, and have been clinically stable without hospital admission for HF in the preceding 3 months. Eligible patients will be randomly assigned, in a 1:1 ratio, to receive a loading and maintenance dose of either nebivolol or carvedilol. Echocardiographic evaluations will be performed at baseline, 6, and 12 months after therapy. Clinical assessment and laboratory tests are to be performed at fixed times. DISCUSSION: This trial is a single-center study that aims to evaluate the impact of nebivolol on LV diastolic function. The results of the study will provide information about the optimal choice of a β-Blocker in the management of patients after diagnosis of HF with preserved EF. The results will be available by 2017. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT02619526 , registered on 25 November 2015.
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Park et al. (2016) conducted an RCT in Heart failure with preserved ejection fraction (n=62). Nebivolol vs. Carvedilol 25 mg twice daily was evaluated on Left ventricular diastolic function measured by echocardiography (including mitral inflow velocities, deceleration time, isovolumetric relaxation time, mitral annular velocities, LA volume, and LA strain) at 12 months. This paper is a study protocol for a randomized controlled trial comparing nebivolol and carvedilol in older patients with heart failure and preserved ejection fraction, and contains no results.
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