Effect and Safety of Fexofenadine Hydrochloride vs Placebo in Patients With Acute Myocardial Infaction: A Randomized Clinical Trial

Overview

The purpose of this study was to evaluate the efficacy and safety of fexofenadine hydrochloride on the basis of standard treatment after PCI in STEMI patients.

Background: Cardiac fibrosis caused by acute myocardial infarction is one of the major causes of death for cardiovascular disease patients in China. Previous research found that expression of FMO2 in heart significantly decreased after myocardial infarction. Overexpression of FMO2 in cardiac fibroblasts using lentivirus can reduce collagen deposition and improve cardiac function, which suggest that FMO2 can be a target for treating cardiac fibrosis. The investigators used the FDA drug library to screen drugs that promote FMO2 expression, then validated the top ranked candidate drug and found that fexofenadine hydrochloride had the most significant effect. Animal experiments found that fexofenadine significantly improved the heart function and reduced heart fibrosis in mice after myocardial infarction and has no significant side effects on liver or kidney function. Fexofenadine Hydrochloride is a third-generation H1 receptor antagonist mainly used to treat allergic diseases such as seasonal allergic rhinitis and chronic idiopathic urticarial. However, currently no study evaluates the efficacy and safety of fexofenadine hydrochloride in treating acute myocardial infarction in human. Purpose: The purpose of this study was to evaluate the efficacy and safety of fexofenadine hydrochloride on the basis of standard treatment after PCI in STEMI patients. Study design: This study is a prospective, multi-center, double blind, randomized controlled clinical trial. The study objects are STEMI patients: left ventricular ejection fraction (LVEF)≤50%, and primary PCI was performed. Participants will be randomly assigned to control group and fexofenadine group in a 1:1 ratio. The control group will receive placebo 3 days after primary PCI for 6 months based on the standard treatment. The fexofenadine group will receive fexofenadine hydrochloride 60mg bid 3 days after primary PCI for 6 months on the basis of standard treatment, and both groups will be followed up for 6 months. Outcome measure: The primary outcome is late gadolinium enhancement/left ventricular mass (LGE/LV mass%). The secondary outcomes are left ventricular ejection fraction (LVEF%), left ventricular end-systolic volume/body surface area (LVESV/BSA%), left ventricular end-diastolic volume/body surface area (LVEDV/BSA%), extracellular volume (ECV), intramyocardial hemorrhage (IMH), stroke volume, peri-infarct zone, BNP, VO2 max, SAQ scale score, drug-associated adverse events and incidence of MACE (including cardiac death, myocardial infarction, readmission due to heart failure).

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Eligibility

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Outcomes

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