<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Park KW</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Second-generation drug-eluting stents (DES) have raised the bar of clinical performance. These stents are mostly made from cobalt chromium alloy. A newer generation DES has been developed from platinum chromium alloy, but clinical data regarding the efficacy and safety of the platinum chromium-based everolimus-eluting stent (PtCr-EES) is limited, with no comparison data against the cobalt chromium-based zotarolimus-eluting stent (CoCr-ZES). In addition, an antiplatelet regimen is an integral component of medical therapy after percutaneous coronary intervention (PCI). A 1-week duration of doubling the dose of clopidogrel (double-dose antiplatelet therapy (DDAT)) was shown to improve outcome at 1 month compared with conventional dose in acute coronary syndrome (ACS) patien</pubmed_abstract><journal>Trials</journal><pagination>29</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3342216</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The 'Harmonizing Optimal Strategy for Treatment of coronary artery stenosis - sAfety &amp; effectiveneSS of drug-elUting stents &amp; antiplatelet REgimen' (HOST-ASSURE) trial: study protocol for a randomized controlled trial.</pubmed_title><pmcid>PMC3342216</pmcid><pubmed_authors>Shin ES</pubmed_authors><pubmed_authors>HOST investigators</pubmed_authors><pubmed_authors>Park JJ</pubmed_authors><pubmed_authors>Hwang KK</pubmed_authors><pubmed_authors>Kwon HM</pubmed_authors><pubmed_authors>Chae IH</pubmed_authors><pubmed_authors>Park BE</pubmed_authors><pubmed_authors>Kim HS</pubmed_authors><pubmed_authors>Yoon JH</pubmed_authors><pubmed_authors>Oh JH</pubmed_authors><pubmed_authors>Kang SH</pubmed_authors><pubmed_authors>Kim S</pubmed_authors><pubmed_authors>Park KW</pubmed_authors><pubmed_authors>Moon KW</pubmed_authors><pubmed_authors>Lee SY</pubmed_authors><pubmed_authors>Cha KS</pubmed_authors><pubmed_authors>Park TH</pubmed_authors><pubmed_authors>Rhew JY</pubmed_authors><pubmed_authors>Jeon HK</pubmed_authors><pubmed_authors>Jeong MH</pubmed_authors><pubmed_authors>Lee SP</pubmed_authors></additional><is_claimable>false</is_claimable><name>The 'Harmonizing Optimal Strategy for Treatment of coronary artery stenosis - sAfety &amp; effectiveneSS of drug-elUting stents &amp; antiplatelet REgimen' (HOST-ASSURE) trial: study protocol for a randomized controlled trial.</name><description>&lt;h4>Background&lt;/h4>Second-generation drug-eluting stents (DES) have raised the bar of clinical performance. These stents are mostly made from cobalt chromium alloy. A newer generation DES has been developed from platinum chromium alloy, but clinical data regarding the efficacy and safety of the platinum chromium-based everolimus-eluting stent (PtCr-EES) is limited, with no comparison data against the cobalt chromium-based zotarolimus-eluting stent (CoCr-ZES). In addition, an antiplatelet regimen is an integral component of medical therapy after percutaneous coronary intervention (PCI). A 1-week duration of doubling the dose of clopidogrel (double-dose antiplatelet therapy (DDAT)) was shown to improve outcome at 1 month compared with conventional dose in acute coronary syndrome (ACS) patien</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Mar</publication><modification>2026-04-07T17:49:05.964Z</modification><creation>2019-03-27T00:52:56Z</creation></dates><accession>S-EPMC3342216</accession><cross_references><pubmed>22463698</pubmed><doi>10.1186/1745-6215-13-29</doi></cross_references></HashMap>