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<?xml-stylesheet type="text/xsl" media="screen" href="/~d/styles/rss2full.xsl"?><?xml-stylesheet type="text/css" media="screen" href="http://feeds.feedburner.com/~d/styles/itemcontent.css"?><rss xmlns:feedburner="http://rssnamespace.org/feedburner/ext/1.0" version="2.0"><channel><title>Clinical Trials</title><link>http://www.cardiosource.org/sitecore%20modules/web/rss/createfeed.aspx?feed=ClinicalTrials</link><description>RSS feed of the most recent clinical trials.</description><copyright>Copyright 2010 ACC.org. All rights reserved.</copyright><atom10:link xmlns:atom10="http://www.w3.org/2005/Atom" rel="self" type="application/rss+xml" href="http://feeds.feedburner.com/cardiosource/yPxP" /><feedburner:info uri="cardiosource/ypxp" /><atom10:link xmlns:atom10="http://www.w3.org/2005/Atom" rel="hub" href="http://pubsubhubbub.appspot.com/" /><item><title>Third International Stroke Trial</title><description>&lt;p&gt;The goal of the trial was to evaluate treatment with intravenous thrombolytic therapy compared with control among a broad range of patients presenting within 6 hours from onset of ischemic stroke.&lt;/p&gt;&lt;img src="http://feeds.feedburner.com/~r/cardiosource/yPxP/~4/g9aR7DaABUs" height="1" width="1"/&gt;</description><link>http://feedproxy.google.com/~r/cardiosource/yPxP/~3/g9aR7DaABUs/IST-3.aspx</link><author>IST-3 Collaborative Group. The benefits and harms of intravenous thrombolysis with recombinant tissue plasminogen activator within 6 h of acute ischaemic stroke (the third international stroke trial [IST-3]): a randomised controlled trial. &lt;a href="http://www.thelancet.com/journals/lancet/article/PIIS0140-6736(12)60768-5/fulltext"&gt;&lt;em&gt;Lancet&lt;/em&gt; 2012;May 23:[Epub ahead of print].&lt;/a&gt;</author><pubDate>2012-05-23 23:11:00</pubDate><feedburner:origLink>http://www.cardiosource.org/Science-And-Quality/Clinical-Trials/I/IST-3.aspx</feedburner:origLink></item><item><title>Aspirin for the Prevention of Recurrent Venous Thromboembolism (Warfarin and Aspirin)</title><description>&lt;p&gt;The goal of the trial was to evaluate treatment with aspirin compared with placebo among patients with treated venous thromboembolism.&lt;/p&gt;&lt;img src="http://feeds.feedburner.com/~r/cardiosource/yPxP/~4/wAYu0pRxhTU" height="1" width="1"/&gt;</description><link>http://feedproxy.google.com/~r/cardiosource/yPxP/~3/wAYu0pRxhTU/WARFASA.aspx</link><author>Becattini C, Agnelli G, Schenone A, et al., on behalf of the WARFASA Investigators. Aspirin for Preventing the Recurrence of Venous Thromboembolism. &lt;a href="http://www.nejm.org/doi/full/10.1056/NEJMoa1114238"&gt;&lt;em&gt;N Engl J Med &lt;/em&gt;2012;366:1959-67&lt;/a&gt;.</author><pubDate>2012-05-23 12:34:00</pubDate><feedburner:origLink>http://www.cardiosource.org/Science-And-Quality/Clinical-Trials/W/WARFASA.aspx</feedburner:origLink></item><item><title>Warfarin Versus Aspirin in Reduced Cardiac Ejection Fraction</title><description>&lt;p&gt;Chronic systolic heart failure (CHF) is associated with a hypercoagulable state. Earlier trials on the use of warfarin in patients with CHF had included patients with atrial fibrillation (AF) and valvular heart disease, and thus, the true value of anticoagulation in patients with CHF but no other obvious cause for anticoagulation is unknown. Accordingly, the WARCEF trial sought to compare outcomes between the use of warfarin and aspirin in patients with CHF and normal sinus rhythm (NSR).&lt;/p&gt;&lt;img src="http://feeds.feedburner.com/~r/cardiosource/yPxP/~4/eJ6iU0tLB7k" height="1" width="1"/&gt;</description><link>http://feedproxy.google.com/~r/cardiosource/yPxP/~3/eJ6iU0tLB7k/WARCEF.aspx</link><author>Homma S, Thompson JL, Pullicino PM, et al. Warfarin and aspirin in patients with heart failure and sinus rhythm. &lt;a href="http://www.nejm.org/doi/full/10.1056/NEJMoa1202299"&gt;&lt;em&gt;N Engl J Med &lt;/em&gt;2012;May 2:[Epub ahead of print].&lt;/a&gt;</author><pubDate>2012-05-14 12:27:00</pubDate><feedburner:origLink>http://www.cardiosource.org/Science-And-Quality/Clinical-Trials/W/WARCEF.aspx</feedburner:origLink></item><item><title>Randomized and Clinical Effectiveness Trial Comparing Two Pharmacogenetic Algorithms and Standard Care for Individualizing Warfarin Dosing</title><description>Warfarin is a commonly prescribed medication that has a narrow therapeutic range, with marked interpatient variability in PK and PD. Pharmacogenetic (PG) studies have identified two genes, &lt;em&gt;CYP2C9&lt;/em&gt; (cytochrome p450 isoform) and &lt;em&gt;VKORC1&lt;/em&gt; (vitamin K epoxide reductase complex subunit 1), to consistently determine warfarin dose requirements. However, studies incorporating genotype analysis and tailored therapy have been inconsistent. The current trial sought to study the safety and efficacy of two PG algorithms on the ability to achieve therapeutic anticoagulation with warfarin.&lt;img src="http://feeds.feedburner.com/~r/cardiosource/yPxP/~4/XGx2xX8d6Qw" height="1" width="1"/&gt;</description><link>http://feedproxy.google.com/~r/cardiosource/yPxP/~3/XGx2xX8d6Qw/CoumaGen-II.aspx</link><author>Anderson JL, Horne BD, Stevens SM, et al. A randomized and clinical effectiveness trial comparing two pharmacogenetic algorithms and standard care for individualizing warfarin dosing (CoumaGen-II). &lt;a href="http://circ.ahajournals.org/content/125/16/1997.abstract"&gt;&lt;em&gt;Circulation &lt;/em&gt;2012;125:1997-2005&lt;/a&gt;.</author><pubDate>2012-05-12 14:31:00</pubDate><feedburner:origLink>http://www.cardiosource.org/Science-And-Quality/Clinical-Trials/C/CoumaGen-II.aspx</feedburner:origLink></item><item><title>Testing platelet Reactivity In patients underGoing elective stent placement on clopidogrel to Guide alternative thErapy with pRasugrel</title><description>&lt;p&gt;The TRIGGER-PCI trial sought to study whether treatment with prasugrel in nonresponders to clopidogrel would be associated with an improvement in platelet reactivity testing on follow-up.&lt;/p&gt;&lt;img src="http://feeds.feedburner.com/~r/cardiosource/yPxP/~4/Smwt_9a2H90" height="1" width="1"/&gt;</description><link>http://feedproxy.google.com/~r/cardiosource/yPxP/~3/Smwt_9a2H90/TRIGGER-PCI.aspx</link><author>
		&lt;p&gt;Trenk D, Stone GW, Gawaz M, et al. A randomized trial of prasugrel versus clopidogrel in patients with high platelet reactivity on clopidogrel after elective percutaneous coronary intervention with implantation of drug-eluting stents: results of the TRIGGER-PCI (Testing Platelet Reactivity In Patients Undergoing Elective Stent Placement on Clopidogrel to Guide Alternative Therapy With Prasugrel) study. &lt;a href="http://content.onlinejacc.org/cgi/content/full/j.jacc.2012.02.026"&gt;&lt;em&gt;J Am Coll Cardiol&lt;/em&gt; 2012;Apr 18:[Epub ahead of print]&lt;/a&gt;.&lt;/p&gt;
    &lt;p&gt;Presented by Dr. Dietmar Trenk at the Transcatheter Cardiovascular Therapeutics meeting (TCT 2011), San Francisco, CA, November 9, 2011.&lt;/p&gt;</author><pubDate>2012-04-18 16:45:00</pubDate><feedburner:origLink>http://www.cardiosource.org/Science-And-Quality/Clinical-Trials/T/TRIGGER-PCI.aspx</feedburner:origLink></item><item><title>PROlonging Dual antiplatelet treatment after Grading stent-induced Intimal hyperplasia studY</title><description>&lt;p&gt;Current guidelines recommend that dual antiplatelet therapy (DAPT) with aspirin and a thienopyridine be continued for a minimum of 12 months following drug-eluting stent (DES) percutaneous coronary intervention (PCI). This recommendation comes from data from numerous observational studies suggesting that early DAPT discontinuation is associated with an increased risk of stent thrombosis. However, randomized controlled data to support this recommendation are lacking. Accordingly, the PRODIGY investigators sought to study if 24 months of DAPT is superior to 6 months of DAPT in all-comers undergoing PCI with both DES and bare-metal stents (BMS).&lt;/p&gt;&lt;img src="http://feeds.feedburner.com/~r/cardiosource/yPxP/~4/PvglmplPk5Y" height="1" width="1"/&gt;</description><link>http://feedproxy.google.com/~r/cardiosource/yPxP/~3/PvglmplPk5Y/PRODIGY.aspx</link><author>
		&lt;p&gt;Valgimigli M, Campo G, Monti M, et al., on behalf of the PROlonging Dual antiplatelet treatment after Grading stent-induced Intimal hyperplasia studY (PRODIGY) Investigators. Short- Versus Long-Term Duration of Dual Antiplatelet Therapy After Coronary Stenting: A Randomized Multicentre Trial. &lt;a href="http://circ.ahajournals.org/content/early/2012/03/16/CIRCULATIONAHA.111.071589.abstract"&gt;&lt;em&gt;Circulation &lt;/em&gt;2012;Mar 21:[Epub ahead of print]&lt;/a&gt;.&lt;/p&gt;
    &lt;p&gt;Presented by Dr. Marco Valgimigli at the European Society of Cardiology Congress, Paris, France, August 2011.&lt;/p&gt;</author><pubDate>2012-04-10 14:05:00</pubDate><feedburner:origLink>http://www.cardiosource.org/Science-And-Quality/Clinical-Trials/P/PRODIGY.aspx</feedburner:origLink></item><item><title>Randomized Trial of Tenecteplase Versus Alteplase for Acute Ischemic Stroke</title><description>&lt;p&gt;Current guidelines recommend that intravenous alteplase (tPA) be administered for systemic fibrinolysis in patients presenting with acute ischemic stroke within 3 hours (Grade I) and within 4.5 hours (Grade IIC) of onset of symptoms. Tenecteplase (TNK) is a genetically modified version of tPA that has some pharmacokinetic benefits over tPA. The current phase II trial sought to compare outcomes in patients with acute ischemic stroke randomized to receive two low doses of TNK versus standard dose of tPA.&lt;/p&gt;&lt;img src="http://feeds.feedburner.com/~r/cardiosource/yPxP/~4/-Eij6hpffa0" height="1" width="1"/&gt;</description><link>http://feedproxy.google.com/~r/cardiosource/yPxP/~3/-Eij6hpffa0/Tenecteplase-Versus-Alteplase-for-Acute-Ischemic-Stroke.aspx</link><author>Parsons M, Spratt N, Bivard A, et al. A randomized trial of tenecteplase versus alteplase for acute ischemic stroke. &lt;a href="http://www.nejm.org/doi/full/10.1056/NEJMoa1109842"&gt;&lt;em&gt;N Engl J Med &lt;/em&gt;2012;366:1099-107&lt;/a&gt;.</author><pubDate>2012-04-10 13:53:00</pubDate><feedburner:origLink>http://www.cardiosource.org/Science-And-Quality/Clinical-Trials/T/Tenecteplase-Versus-Alteplase-for-Acute-Ischemic-Stroke.aspx</feedburner:origLink></item><item><title>Clopidogrel for High Atherothrombotic Risk, Ischemic Stabilization, Management, and Avoidance</title><description>The goal of the trial was to evaluate antiplatelet treatment with aspirin alone compared with aspirin plus clopidogrel among high-risk patients with stable cardiovascular (CV) disease.&lt;img src="http://feeds.feedburner.com/~r/cardiosource/yPxP/~4/n_-clW1S_jI" height="1" width="1"/&gt;</description><link>http://feedproxy.google.com/~r/cardiosource/yPxP/~3/n_-clW1S_jI/CHARISMA.aspx</link><author>
		&lt;p&gt;Bhatt DL, Fox KA, Hacke W, et al. Clopidogrel and aspirin versus aspirin alone for the prevention of atherothrombotic events. &lt;a href="http://www.nejm.org/doi/full/10.1056/NEJMoa060989"&gt;&lt;em&gt;N Engl J Med &lt;/em&gt;2006;354:1706-17&lt;/a&gt;.&lt;/p&gt;
    &lt;p&gt;
      &lt;em&gt;Post-hoc analysis: &lt;/em&gt;Bhatt DL, Paré G, Eikelboom JW, et al., on behalf of the CHARISMA Investigators. The Relationship Between &lt;em&gt;CYP2C19&lt;/em&gt; Polymorphisms and Ischemic and Bleeding Outcomes in Stable Outpatients: The CHARISMA Genetics Study. &lt;a href="http://eurheartj.oxfordjournals.org/content/early/2012/03/25/eurheartj.ehs059.abstract"&gt;&lt;em&gt;Eur Heart J&lt;/em&gt; 2012;Mar 26:[Epub ahead of print]&lt;/a&gt;. &lt;/p&gt;
    &lt;p&gt;Presented by Dr. Deepak L. Bhatt at the March 2006 ACC Annual Scientific Session, Atlanta, GA. &lt;br /&gt;&lt;br /&gt;&lt;/p&gt;</author><pubDate>2012-04-05 17:00:00</pubDate><feedburner:origLink>http://www.cardiosource.org/Science-And-Quality/Clinical-Trials/C/CHARISMA.aspx</feedburner:origLink></item><item><title>Reassessment of Anti-Platelet Therapy Using an Individualized Strategy Based on Genetic Evaluation</title><description>The goal of the trial was to evaluate a strategy of rapid genotyping for the &lt;em&gt;CYP2C19*2&lt;/em&gt; allele with selective use of prasugrel (in carriers of the &lt;em&gt;CYP2C19*2&lt;/em&gt; allele) compared with standard therapy with clopidogrel (in noncarriers of the &lt;em&gt;CYP2C19*2&lt;/em&gt; allele) among patients undergoing percutaneous coronary intervention (PCI).&lt;img src="http://feeds.feedburner.com/~r/cardiosource/yPxP/~4/ROjzf9qSaBQ" height="1" width="1"/&gt;</description><link>http://feedproxy.google.com/~r/cardiosource/yPxP/~3/ROjzf9qSaBQ/RAPID-GENE.aspx</link><author>
		&lt;p&gt;Roberts JD, Wells GA, Le May MR, et al. Point-of-care genetic testing for personalisation of antiplatelet treatment (RAPID-GENE): a prospective, randomised, proof-of-concept trial. &lt;a href="http://www.thelancet.com/journals/lancet/article/PIIS0140-6736(12)60161-5/abstract"&gt;&lt;em&gt;Lancet&lt;/em&gt; 2012;Mar 28:[Epub ahead of print]&lt;/a&gt;.&lt;/p&gt;
    &lt;p&gt;Presented by Dr. Derek So at the Transcatheter Cardiovascular Therapeutics meeting (TCT 2011), San Francisco, CA, November 9, 2011.&lt;/p&gt;</author><pubDate>2012-04-03 21:38:00</pubDate><feedburner:origLink>http://www.cardiosource.org/Science-And-Quality/Clinical-Trials/R/RAPID-GENE.aspx</feedburner:origLink></item><item><title>Moderate Pulmonary Embolism Treated With Thrombolysis</title><description>&lt;p&gt;The goal of the trial was to evaluate treatment with low-dose thrombolytic therapy compared with usual care among patients with hemodynamically stable moderate pulmonary embolism (PE).&lt;/p&gt;&lt;img src="http://feeds.feedburner.com/~r/cardiosource/yPxP/~4/JbFbGZhHj7k" height="1" width="1"/&gt;</description><link>http://feedproxy.google.com/~r/cardiosource/yPxP/~3/JbFbGZhHj7k/MOPETT.aspx</link><author>
		&lt;p&gt;Presented by Dr. Mohsen Sharifi at ACC.12 &amp;amp; ACC-i2 with TCT, Chicago, IL, March 27, 2012.&lt;/p&gt;
</author><pubDate>2012-03-27 00:57:00</pubDate><feedburner:origLink>http://www.cardiosource.org/Science-And-Quality/Clinical-Trials/M/MOPETT.aspx</feedburner:origLink></item><item><title>Immediate Myocardial Metabolic Enhancement During Initial Assessment and Treatment in Emergency Care</title><description>&lt;p&gt;The goal of the trial was to evaluate treatment with intravenous glucose, insulin, and potassium (GIK) compared with placebo when given early during a suspected acute coronary syndrome (ACS).&lt;/p&gt;&lt;img src="http://feeds.feedburner.com/~r/cardiosource/yPxP/~4/7iKjvmhFTPw" height="1" width="1"/&gt;</description><link>http://feedproxy.google.com/~r/cardiosource/yPxP/~3/7iKjvmhFTPw/IMMEDIATE.aspx</link><author>
		&lt;p&gt;Selker HP, Beshansky JR, Sheehan PR, et al. Out-of-Hospital Administration of Intravenous Glucose-Insulin-Potassium in Patients With Suspected Acute Coronary Syndromes: The IMMEDIATE Randomized Controlled Trial. &lt;a href="http://jama.ama-assn.org/content/early/2012/03/21/jama.2012.426.full"&gt;&lt;em&gt;JAMA&lt;/em&gt; 2012;Mar 27:[Epub ahead of print]&lt;/a&gt;.&lt;/p&gt;
    &lt;p&gt;Presented by Dr. Harry Selker at ACC.12 &amp;amp; ACC-i2 with TCT, Chicago, IL, March 27, 2012. &lt;br /&gt;&lt;/p&gt;</author><pubDate>2012-03-27 00:44:00</pubDate><feedburner:origLink>http://www.cardiosource.org/Science-And-Quality/Clinical-Trials/I/IMMEDIATE.aspx</feedburner:origLink></item><item><title>Rule Out Myocardial Ischemia/Infarction Using Computer Assisted Tomography</title><description>&lt;p&gt;The goal of the trial was to evaluate a strategy of cardiac computed tomography (CT) angiography compared with standard emergency department (ED) evaluation among patients with suspected acute coronary syndrome (ACS).&lt;/p&gt;&lt;img src="http://feeds.feedburner.com/~r/cardiosource/yPxP/~4/-vGcsV1CZ2s" height="1" width="1"/&gt;</description><link>http://feedproxy.google.com/~r/cardiosource/yPxP/~3/-vGcsV1CZ2s/ROMICAT-II.aspx</link><author>
		&lt;p&gt;Presented by Dr. Udo Hoffmann at ACC.12 &amp;amp; ACC-i2 with TCT, Chicago, IL, March 27, 2012.&lt;/p&gt;
</author><pubDate>2012-03-27 00:35:00</pubDate><feedburner:origLink>http://www.cardiosource.org/Science-And-Quality/Clinical-Trials/R/ROMICAT-II.aspx</feedburner:origLink></item><item><title>EINSTEIN–Pulmonary Embolism (PE) Study</title><description>&lt;p&gt;The goal of the trial was to evaluate treatment of the oral direct factor Xa inhibitor, rivaroxaban, compared with standard therapy among patients with symptomatic pulmonary embolism (PE).&lt;/p&gt;&lt;img src="http://feeds.feedburner.com/~r/cardiosource/yPxP/~4/wJl47CGme6U" height="1" width="1"/&gt;</description><link>http://feedproxy.google.com/~r/cardiosource/yPxP/~3/wJl47CGme6U/EINSTEIN-PE.aspx</link><author>The EINSTEIN–PE Investigators. Oral rivaroxaban for the treatment of symptomatic pulmonary embolism. &lt;em&gt;N Engl J Med&lt;/em&gt; 2012;Mar 26:[Epub ahead of print]. &lt;br /&gt;&lt;br /&gt;Presented by Dr. Harry Buller at ACC.12 &amp;amp; ACC-i2 with TCT, Chicago, IL, March 24, 2012. &lt;br /&gt;</author><pubDate>2012-03-26 15:33:00</pubDate><feedburner:origLink>http://www.cardiosource.org/Science-And-Quality/Clinical-Trials/E/EINSTEIN-PE.aspx</feedburner:origLink></item><item><title>CT Angiography for Safe Discharge of Patients With Possible Acute Coronary Syndromes</title><description>&lt;p&gt;The goal of the trial was to evaluate a strategy of cardiac computed tomography (CT) angiography compared with traditional care among low- to intermediate-risk patients with possible acute coronary syndrome (ACS).&lt;/p&gt;&lt;img src="http://feeds.feedburner.com/~r/cardiosource/yPxP/~4/dnotBi7d4Dk" height="1" width="1"/&gt;</description><link>http://feedproxy.google.com/~r/cardiosource/yPxP/~3/dnotBi7d4Dk/ACRIN-PA-4005.aspx</link><author>Litt HI, Gatsonis C, Snyder B, et al. CT angiography for safe discharge of patients with possible acute coronary syndromes. &lt;a href="http://www.nejm.org/doi/full/10.1056/NEJMoa1201163?query=featured_home"&gt;&lt;em&gt;N Engl J Med &lt;/em&gt;2012;Mar 26:[Epub ahead of print]&lt;/a&gt;. &lt;br /&gt;&lt;br /&gt;Presented by Dr. Harold Litt at ACC.12 &amp;amp; ACC-i2 with TCT, Chicago, IL, March 26, 2012. &lt;br /&gt;&lt;br /&gt;</author><pubDate>2012-03-26 14:46:00</pubDate><feedburner:origLink>http://www.cardiosource.org/Science-And-Quality/Clinical-Trials/A/ACRIN-PA-4005.aspx</feedburner:origLink></item><item><title>CABG Off or On Pump Revascularization Study</title><description>&lt;p&gt;The goal of the trial was to evaluate off-pump compared with on-pump technique among patients undergoing coronary artery bypass grafting (CABG).&lt;/p&gt;&lt;img src="http://feeds.feedburner.com/~r/cardiosource/yPxP/~4/otIZn1J-ewY" height="1" width="1"/&gt;</description><link>http://feedproxy.google.com/~r/cardiosource/yPxP/~3/otIZn1J-ewY/CORONARY.aspx</link><author>Lamy A, Devereaux PJ, Prabhakaran D, et al., on behalf of the CORONARY Investigators. Off-Pump or On-Pump Coronary Artery Bypass Grafting at 30 days. &lt;a href="http://www.nejm.org/doi/full/10.1056/NEJMoa1200388?query=featured_home"&gt;&lt;em&gt;N Engl J Med &lt;/em&gt;2012;Mar 26:[Epub ahead of print]&lt;/a&gt;. &lt;br /&gt;&lt;br /&gt;Presented by Dr. Andre Lamy at ACC.12 &amp;amp; ACC-i2 with TCT, Chicago, IL, March 26, 2012. &lt;br /&gt;</author><pubDate>2012-03-26 13:38:00</pubDate><feedburner:origLink>http://www.cardiosource.org/Science-And-Quality/Clinical-Trials/C/CORONARY.aspx</feedburner:origLink></item></channel></rss>

