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<oembed><version>1.0</version><provider_name>The Texas Heart Institute&#xAE;</provider_name><provider_url>https://www.texasheart.org</provider_url><author_name>Daynene Vykoukal</author_name><author_url>https://www.texasheart.org/author/daynene/</author_url><title>BiVACOR (NCT06174103)</title><type>rich</type><width>600</width><height>338</height><html>&lt;blockquote class="wp-embedded-content" data-secret="2P7ZjSHBuI"&gt;&lt;a href="https://www.texasheart.org/research/clinical-trials/bivacor-nct06174103/"&gt;BiVACOR (NCT06174103)&lt;/a&gt;&lt;/blockquote&gt;&lt;iframe sandbox="allow-scripts" security="restricted" src="https://www.texasheart.org/research/clinical-trials/bivacor-nct06174103/embed/#?secret=2P7ZjSHBuI" width="600" height="338" title="&#x201C;BiVACOR (NCT06174103)&#x201D; &#x2014; The Texas Heart Institute&#xAE;" data-secret="2P7ZjSHBuI" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"&gt;&lt;/iframe&gt;&lt;script type="text/javascript"&gt;
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</html><description>The purpose of this study is to assess the feasibility of using the BiVACOR Total Artificial Heart (TAH) System to support adult patients with severe biventricular heart failure, or univentricular heart failure in which left ventricular assist device (LVAD) support is not recommended, who require mechanical circulatory support to sustain life. Feasibility will be assessed by evaluating safety and performance of the BiVACOR TAH System in study subjects.</description><thumbnail_url>https://www.texasheart.org/wp-content/uploads/2018/01/forefront-of-discovery.jpg</thumbnail_url><thumbnail_width>2048</thumbnail_width><thumbnail_height>1083</thumbnail_height></oembed>
