Efficacy of Esmolol in the Identification of Cardiovascular Disorders by Cirrhosis, Diabetes Mellitus and Cardiotoxic Treatments

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorConsorcio Centro de Investigación Biomédica en Red (CIBER)

About this trial

The purpose of this study is to assess the superiority of esmolol echocardiography over conventional echocardiography in the diagnosis of subclinical myocardial involvement associated with diabetes mellitus 2, cirrhosis and antineoplastic treatments.

Eligibility criteria

Qualifiers

Age ≥ 18 years.

Absence of previous heart disease, defined as the absence of relevant cardiac structural alterations such as moderate or severe hypertrophy, alteration of segmental contraction, Moderate or severe valvular disease, intraventricular obstructive gradient, or old myocardial infarction.

Existence of an at least acceptable ultrasonic window, which allows the visualization of at least 14 of the 17 segments of the LV myocardium.

Sinus rhythm, with a basal heart rate greater than 50 bpm.

Disqualifiers

Contraindication for the administration of esmolol (according to technical data sheet): Hypersensitivity to esmolol hydrochloride; Severe sinus bradycardia (HR <50 bpm); 2nd or 3rd degree atrioventricular block without pacemaker; Cardiogenic shock, severe hypotension, or decompensated heart failure; Untreated pheochromocytoma; Acute asthmatic attack; Concomitant intravenous administration or within the first 48 hours after verapamil.

Treatment with beta-blocker drugs (oral, topical or intravenous) in the last 7 days before the study.

History of ventricular or supraventricular arrhythmias that prevent the safe withdrawal of antiarrhythmic or braking treatment before the administration of esmolol.

History of previous high-grade atrioventricular (AV) conduction disorder in non-pacemaker patients.

Trial design

Treatments tested in this trial

  • Esmolol Injection [Brevibloc]

Treatment groups

1,000 Participants
are divided into 1 treatment group

Sponsors and collaborators