Ivabradine in Patients With Congestive Heart Failure

Damanhour University60 enrolled

Overview

The aim of this study is to assess the efficacy of Ivabradine therapy in patients with congestive heart failure using the cardiac biomarkers NT-Pro BNP and Neopterin.

* Approval will be obtained from Research Ethics Committee of Faculty of Pharmacy, Damanhour University * All participants have agreed to take part in this clinical study and provide informed consent * A 3 months, prospective interventional study. * Sixty ambulatory, clinically stable symptomatic patients with systolic chronic HF (≥ 4 weeks), on optimized standard medical therapy were consecutively included and randomly allocated to the ivabradine group (n=30) and non-ivabradine group (n=30). * The baseline evaluation comprised physical examination, NYHA class, 12-lead electrocardi¬ography (ECG), Echocardiography, blood sampling for laboratory measurements, including NT-Pro BNP and Neopterin. * Patients in the Ivabradine group were administered Ivabradine 5 mg twice daily and doses (2.5, 5, 7.5 mg) were to be adjusted upwards or downwards at every visit according to HR at rest and tolerability. * Patients were followed up after 1 week of initiation of ivabradine therapy then monthly till the end of the study. * Peripheral venous blood samples were drawn between 8 and 9 am after a 30-min rest in the supine position. Serum samples were frozen at -80°C until assay. * Levels of NT-Pro BNP and Neopterin were detected using ELISA kits as prescribed by manufacturer. * Statistical tests appropriate to the study will be conducted to evaluate significance of results * Results, conclusion, discussion and recommendations will be given

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

Conditions

Congestive Heart Failure

Interventions

Ivabradine Oral TabletDRUG

Ivabradine 5 mg twice daily and doses (2.5, 5, 7.5 mg) were to be adjusted upwards or downwards at every visit according to HR at rest and tolerability plus their standard treatment.

Blacebo plus standard treatmentDRUG

Blacebo plus standard treatment

Eligibility

Sex: ALLMin age: 30 YearsMax age: 70 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Patients with chronic HF, on optimized medical therapy according to European Society of Cardiol¬ogy guidelines, with LV ejection fraction (LVEF) \< 35% according to the Simpson method, New York Heart Association (NYHA) class II-III, and sinus rhythm and resting HR \> 70/min were eligible for inclusion in the study. Exclusion Criteria: * acute decompen¬sation (acute coronary syndromes and acute HF); * hemodynamically significant valve disease; * cer¬ebrovascular events during the previous 6 months; * dysfunctional prosthetic heart valve; * obstructive or non-obstructive cardiomyopathy; uncorrected congenital heart disease; active myocarditis; * a his¬tory of resuscitation from sudden death; an absence of stable sinus rhythm, severe arrhythmias; HR \< 60 bpm; sick sinus syndrome; second-degree and third-degree atrioventricular block; * severe obesity (body mass index \> 36 kg/m²); * established or sus¬pected pulmonary diseases (vital capacity \< 80% or forced expiratory volume in 1 s \< 80% of age spe¬cific and sex-specific reference values); * hemoglobin ≤ 11 g/dL; * treatment with non-dihydropyridine calcium-channel blockers, class I antiarrhythmic agents, strong inhibitors of cytochrome P450-3A4, or QT interval-prolonging medications; * acute and chronic kidney failure; * pregnancy; hypo- and hy¬perthyroidism or acute infections.

Locations (1)

Tanta University Hospital

Tanta, El-Gharbia, Egypt

Outcomes

Primary Outcomes

NT-Pro BNP

Serum BNP (pg/ml)

Time frame: three months

Neopterin

Serum Neopterin (nmol/L)

Time frame: three months

Secondary Outcomes

Heart Rate

Heart Rate (Beat/Minute)

Time frame: Three Months

Data from ClinicalTrials.gov

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