Antazoline in Comparison to Propafenone in Pharmacological Cardioversion of Atrial Fibrillation.

Atrial Fibrillation Clinical Trial

— AnProAF  

Official title:

Clinical Efficacy and Safety of Antazoline in Comparison to Propafenone in Conversion of Paroxysmal Atrial Fibrillation to Sinus Rhythm - a Single Center, Randomized, Double-blinded Study (the AnProAF Study).

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05720572
• Other study ID #: CMKP/85/PB/2019
• Status: Recruiting
• Phase: Phase 4
• Start date: September 1, 2019
• Est. completion date: January 1, 2026

Study information

• Verified date: February 2023
• Source: Centre of Postgraduate Medical Education
• Contact: Jaroslaw JK Karwowski, PhD
• Phone: +48502913169
• Email: karwowski.jarek[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this randomized, double blind, non-inferiority clinical trial was to compare the clinical efficacy and safety of antazoline with propafenone in the rapid conversion of paroxysmal non-valvular atrial fibrillation to sinus rhythm in patients without heart failure

Description:

Background

Atrial fibrillation (AF) is the most common type of arrhythmia, and occurs in approximately 3% of the population over 20 years of age and 9% of those over 80 years of age [1]. Restoration of sinus rhythm (SR) remains an integral part of the treatment for this type of arrhythmia. Early pharmacological (PCV) or electrical cardioversion (ECV) is necessary to improve symptoms, prevent the side effects of the prolonged crisis of arrhythmia, and avoid hospitalization. ECV requires general sedation and does not prevent from immediate AF recurrence. Therefore, the majority of patients are qualified for pharmacological attempts to terminate the arrhythmia. The early PCV of AF to SR may be achieved by administration of Class (Vaughan-Williams) IA, IC, and III antiarrhythmic drugs (AADs): flecainide, ibutilide, dofetilide, propafenone, amiodarone, or novel agent vernakalant. These AADs have limitations such as proarrhythmic side effects in patients with structural heart disease (IC), delayed onset of action (amiodarone), high cost, and low availability (vernakalant) [1].

An efficacious, well-tolerated, less expensive antiarrhythmic drug with rapid onset of action is necessary. Antazoline meslate is an antihistaminic agent with antiarrhythmic quinidine-like properties, which have been documented in 1960s [2,3]. Electrophysiologically, antazoline prolongs action potential duration and lowers its amplitude, prolongs phase-0 duration, reduces phase-4 of resting potential, and reduces excitability of cardiac tissue. Anticholinergic action of this drug leads to transient increase of heart rate, improving atrioventricular conduction and increasing the corrected QT-interval, left atrial refractory period, and inter-atrial conduction time [4-6]. In human healthy volunteers, the terminal elimination half-life of antazoline was 2.29 hours with a mean residence time of 3.45 hours [7]. In clinical practice, the drug can be administered intravenously in boluses of 50-100 mg every 3-5 minutes until successful cardioversion or up to a cumulative dose of 250-350 mg [8].

In Poland, it was registered for intravenous termination of supraventricular arrhythmias. Unfortunately, antazoline is not listed in any of the formal guidelines due to the lack of large randomized trials comparing this drug with other AADs in SR restoration. To the best of our knowledge, only one randomized clinical trial has been published that evaluated the antiarrhythmic effect of antazoline in comparison to placebo [9]. In antazoline group (38 patients), successful conversion of AF to SR was achieved in 72.2%, with a median duration of 16 minutes. Other published observational studies have shown high efficacy of antazoline, ranging between 50% and 80% and a rapid onset of action with cardioversion duration between 7 and 20 minutes [3,8,10-14]. The aim of this randomized, double blind, placebo-controlled, non-inferiority clinical trial is to assess clinical efficacy of antazoline in rapid conversion of atrial fibrillation to sinus rhythm in patients with paroxysmal atrial fibrillation without significant valvular disease or advanced heart failure.

Methods Study objectives The purpose of the study is to assess clinical efficacy of antazoline in rapid conversion of AF to SR in comparison to propafenone in patients with paroxysmal atrial fibrillation without significant valvular disease or advanced heart failure. Due to a presumed lack of statistical power, secondary end points and safety analysis will be considered exploratory.

Study design This randomized, double-blind, placebo-controlled, non-inferiority clinical study is actually carried out at the Department of Heart Disease, Centre of Postgraduate Medical Education, Warsaw, Poland. The study will include 390 participants presenting with an episode of AF lasting less than 48 h. All participants must sign an informed consent form. Approval for the study was obtained from the local ethics committee (nr 85/PB/2019; July 10, 2019).

The study protocol was approved by the local ethics committee and is in full compliance with the Declaration of Helsinki.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 105
• Est. completion date: January 1, 2026
• Est. primary completion date: September 1, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 90 Years

Eligibility

Inclusion Criteria:

• Written informed consent for participating in the study and written standard version of informed consent for cardioversion accepted at the Department of Heart Disease, Warsaw, Poland

• Age 18 to 90years

• AF lasting < 48 hours

• Stable cardio-pulmonary state on enrollment

• In case of unclear history of heart failure or suspicion of left ventricle damage echocardiographyis indicated prior to enrollment

Exclusion Criteria:

• Lack of written informed consent

• Allergy to antazoline or propafenone

• Intolerance of anatzoline or propafenone

• AF related to significant valvular disease

• Clinically significant heart failure or ejection fraction <50%

• Systolic blood pressure (BP) <100 mmHg

• History of significant bradyarrhythmia not treatedwith permanent pacemaker

• Resting ventricular rate of < 80 bpm without pacemaker backup

• Heart rate > 140 bpm

• Tachycardia >160'

• Advanced liver or kidney failure

• Acute coronary syndrome, coronary artery by-passgraft, stroke or transient ischemic attack within 30 days before enrollment

• Preexcitation in ECG not treated by radiofrequency ablation of accessory pathway

• Signs and symptoms of ischemia related to AF

• An investigational drug used within 30 days before enrollment

• Advanced liver or kidney failure

• QT prolongation over 440 ms or QTc (Bazett's formula) over the population norm

• Pregnancy or breast feeding

• Background therapy of any oral AADs.

Related Conditions & MeSH terms

• Atrial Fibrillation

Intervention

Drug:
• Antazoline
Participants assigned to the antazoline group will be administered antazoline in boluses in boluses of 100 mg diluted to 20 cm3 every 10 minutes up to a total dose of 300 mg diluted to 60 cm3 or conversion of AF to SR. Drug administration will also be stopped in case of an adverse event or conversion of AF to a different supraventricular arrhythmia. BP will be measured before every injection.
• Propafenone
Patients assigned to the propafenone group were administered three 20-cm3 boluses every 10 minutes up to 60 cm3 or conversion of AF to SR. Each of the first two boluses included 70 mg propafenone (total dose 140 mg), and the third bolus contained only 20-cm3 0.9% NaCl. Drug administration will be stopped in case of an adverse event or conversion of AF to a different supraventricular arrhythmia. BP will be measured before every injection.

Locations

Country	Name	City	State
Poland	Postgraduate Medical School	Warsaw

Sponsors (1)

Lead Sponsor	Collaborator
Centre of Postgraduate Medical Education

Country where clinical trial is conducted

Poland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Conversion of atrial fibrillation (AF) to sinus rhythm (SR)	Conversion of AF to SR confirmed in standard 12-lead ECG during the observation period	3 hours
Secondary	Time to conversion of atrial fibrillation to sinus rhythm		3 hours
Secondary	Serious adverse event defined as every adverse event requiring hospitalization or prolonged observation		3 hours
Secondary	Disturbances of atrioventricular conduction		3 hours
Secondary	Hypotension < 90mmHg		3 hours
Secondary	Pauses > 4s	Pauses in heart beat	3 hours
Secondary	Tachycardia > 180bpm		3 hours
Secondary	Nausea and/or vomiting		3 hours
Secondary	Hot flush		3 hours
Secondary	Drowsiness		3 hours
Secondary	Headache		3 hours
Secondary	Bitter/metallic taste		3 hours
Secondary	Anxiety		3 hours
Secondary	New complex ventricular arrhythmia		3 hours
Secondary	Prolongation of QTc in ms (Bazett's formula) in comparison to baseline		3 hours