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	<title>Ventricular extrasystoles &#8211; European Clinical Trials Information Network</title>
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	<title>Ventricular extrasystoles &#8211; European Clinical Trials Information Network</title>
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		<title>Study of drug combination therapy in asymptomatic patients with frequent premature ventricular contractions and normal heart function to prevent left ventricular dysfunction</title>
		<link>https://clinicaltrials.eu/trial/study-on-the-effect-of-verapamil-and-drug-combination-on-heart-function-in-asymptomatic-patients-with-frequent-premature-ventricular-complexes/</link>
		
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		<pubDate>Wed, 29 Apr 2026 14:59:18 +0000</pubDate>
				<guid isPermaLink="false">https://clinicaltrials.eu/trial/study-on-the-effect-of-verapamil-and-drug-combination-on-heart-function-in-asymptomatic-patients-with-frequent-premature-ventricular-complexes/</guid>

					<description><![CDATA[This study focuses on patients with premature ventricular complexes (PVCs), which are extra, abnormal heartbeats that begin in the heart&#8217;s lower chambers. The study specifically looks at people who have frequent PVCs (more than 10% of total heartbeats) but don&#8217;t feel any symptoms and have normal heart function. Several medications will be tested including verapamil, [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>This study focuses on patients with <b>premature ventricular complexes</b> (PVCs), which are extra, abnormal heartbeats that begin in the heart&#8217;s lower chambers. The study specifically looks at people who have frequent PVCs (more than 10% of total heartbeats) but don&#8217;t feel any symptoms and have normal heart function. Several medications will be tested including <b>verapamil</b>, <b>nebivolol</b>, <b>amiodarone</b>, <b>propafenone</b>, <b>bisoprolol</b>, <b>diltiazem</b>, <b>flecainide</b>, and <b>sotalol</b>.</p>
<p>The purpose is to determine if treating patients who have frequent PVCs but no symptoms can prevent future heart problems better than simply monitoring them without treatment. The study will last for 24 months, during which patients may receive medication or, if necessary, a procedure called <b>ablation</b> (which uses heat to destroy small areas of heart tissue causing irregular rhythms) if medications alone don&#8217;t reduce the PVCs enough.</p>
<p>Throughout the study, doctors will monitor how well the heart is pumping blood using special imaging tests like <b>cardiac magnetic resonance imaging</b> (cMRI) or heart ultrasound. They will also track changes in heart function, measure exercise capacity, and monitor for any side effects from the treatments.</p>
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		<title>Comparison of Carvedilol and Flecainide Treatment in Patients with Idiopathic Ventricular Arrhythmias</title>
		<link>https://clinicaltrials.eu/trial/study-comparing-carvedilol-and-flecainide-for-patients-with-idiopathic-ventricular-arrhythmias/</link>
		
		<dc:creator><![CDATA[]]></dc:creator>
		<pubDate>Wed, 29 Apr 2026 14:30:34 +0000</pubDate>
				<guid isPermaLink="false">https://clinicaltrials.eu/trial/study-comparing-carvedilol-and-flecainide-for-patients-with-idiopathic-ventricular-arrhythmias/</guid>

					<description><![CDATA[This clinical trial focuses on idiopathic ventricular arrhythmias, a heart condition where the heart beats irregularly without a known cause. The study compares two medications: carvedilol and flecainide, which are taken as oral tablets to treat irregular heart rhythms. The purpose is to determine which medication is more effective in reducing irregular heartbeats. Participants will [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>This clinical trial focuses on <b>idiopathic ventricular arrhythmias</b>, a heart condition where the heart beats irregularly without a known cause. The study compares two medications: <b>carvedilol</b> and <b>flecainide</b>, which are taken as oral tablets to treat irregular heart rhythms. The purpose is to determine which medication is more effective in reducing irregular heartbeats.</p>
<p>Participants will receive either carvedilol (up to 50 mg daily) or flecainide (up to 300 mg daily) for a period of 12 months. During the study, heart activity will be monitored using a <b>Holter-ECG</b>, which is a portable device that records heart rhythms over 24 hours. The recordings will be taken before starting treatment and after completing it.</p>
<p>The study will also look at how these medications affect overall quality of life and heart function. Heart function will be evaluated using <b>echocardiography</b>, a test that uses sound waves to create pictures of the heart. The study will track any side effects that participants may experience during the treatment period.</p>
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