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Comparison of the rhythm control treatment strategy versus the rate control strategy in patients with permanent or long-standing persistent atrial fibrillation and heart failure treated with cardiac resynchronization therapy - a pilot study of Cardiac Resynchronization in Atrial Fibrillation Trial (Pilot-CRAfT): study protocol for a randomized controlled trial
The only subgroups of patients with heart failure and atrial fibrillation in which the efficacy of cardiac resynchronization therapy has been scientifically proven are patients with indications for right ventricular pacing and patients after atrioventricular junction ablation. However it is unlikely...
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Published in: | Trials 2014-10, Vol.15 (1), p.386-386, Article 386 |
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creator | Ciszewski, Jan Maciag, Aleksander Kowalik, Ilona Syska, Pawel Lewandowski, Michal Farkowski, Michal M Borowiec, Anna Chwyczko, Tomasz Pytkowski, Mariusz Szwed, Hanna Sterlinski, Maciej |
description | The only subgroups of patients with heart failure and atrial fibrillation in which the efficacy of cardiac resynchronization therapy has been scientifically proven are patients with indications for right ventricular pacing and patients after atrioventricular junction ablation. However it is unlikely that atrioventricular junction ablation would be a standard procedure in the majority of the heart failure patients with cardiac resynchronization therapy and concomitant atrial fibrillation due to the irreversible character of the procedure and a spontaneous sinus rhythm resumption that occurs in about 10% of these patients.
Pilot-CRAfT is the first randomized controlled trial evaluating the efficacy of a rhythm control strategy in atrial fibrillation patients with cardiac resynchronization therapy devices. The aim of this prospective, single center randomized controlled pilot study is to answer the question whether the patients with cardiac resynchronization therapy and permanent atrial fibrillation would benefit from a strategy to restore and maintain sinus rhythm (that is 'rhythm control' strategy) in comparison to rate control strategy. The study population consists of 60 patients with heart failure and concomitant long-standing persistent or permanent atrial fibrillation who underwent a cardiac resynchronization therapy device implantation at least 3 months before qualification. Study participants are randomly assigned to the rhythm control strategy (including electrical cardioversion and pharmacotherapy) or to the rate control group whose goal is to control ventricular rate. The follow-up time is 12 months. The primary endpoint is the ratio of effectively captured biventricular beats. The secondary endpoints include peak oxygen consumption, six-minute walk test distance, heart failure symptom escalation, reverse remodelling of the heart on echo and quality of life.
NCT01850277 registered on 22 April 2013 (ClinicalTrials.gov). |
doi_str_mv | 10.1186/1745-6215-15-386 |
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Pilot-CRAfT is the first randomized controlled trial evaluating the efficacy of a rhythm control strategy in atrial fibrillation patients with cardiac resynchronization therapy devices. The aim of this prospective, single center randomized controlled pilot study is to answer the question whether the patients with cardiac resynchronization therapy and permanent atrial fibrillation would benefit from a strategy to restore and maintain sinus rhythm (that is 'rhythm control' strategy) in comparison to rate control strategy. The study population consists of 60 patients with heart failure and concomitant long-standing persistent or permanent atrial fibrillation who underwent a cardiac resynchronization therapy device implantation at least 3 months before qualification. Study participants are randomly assigned to the rhythm control strategy (including electrical cardioversion and pharmacotherapy) or to the rate control group whose goal is to control ventricular rate. The follow-up time is 12 months. The primary endpoint is the ratio of effectively captured biventricular beats. The secondary endpoints include peak oxygen consumption, six-minute walk test distance, heart failure symptom escalation, reverse remodelling of the heart on echo and quality of life.
NCT01850277 registered on 22 April 2013 (ClinicalTrials.gov).</description><identifier>ISSN: 1745-6215</identifier><identifier>EISSN: 1745-6215</identifier><identifier>DOI: 10.1186/1745-6215-15-386</identifier><identifier>PMID: 25281275</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Anti-Arrhythmia Agents - adverse effects ; Anti-Arrhythmia Agents - therapeutic use ; Atrial Fibrillation - diagnosis ; Atrial Fibrillation - physiopathology ; Atrial Fibrillation - therapy ; Cardiac Resynchronization Therapy - adverse effects ; Catheter Ablation - adverse effects ; Clinical Protocols ; Combined Modality Therapy ; Comparative analysis ; Defibrillators ; Electric Countershock - adverse effects ; Electric Countershock - instrumentation ; Heart Failure - diagnosis ; Heart Failure - physiopathology ; Heart Failure - therapy ; Humans ; Medical research ; Medicine, Experimental ; Pilot Projects ; Poland ; Prospective Studies ; Quality of Life ; Recovery of Function ; Research Design ; Study Protocol ; Time Factors ; Treatment Outcome</subject><ispartof>Trials, 2014-10, Vol.15 (1), p.386-386, Article 386</ispartof><rights>COPYRIGHT 2014 BioMed Central Ltd.</rights><rights>Ciszewski et al.; licensee BioMed Central Ltd. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b593t-bc26f9a83dc99fbf2fae16375f2315ee448fb67395a2e163dcaffb07480fb3ac3</citedby><cites>FETCH-LOGICAL-b593t-bc26f9a83dc99fbf2fae16375f2315ee448fb67395a2e163dcaffb07480fb3ac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283117/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283117/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25281275$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ciszewski, Jan</creatorcontrib><creatorcontrib>Maciag, Aleksander</creatorcontrib><creatorcontrib>Kowalik, Ilona</creatorcontrib><creatorcontrib>Syska, Pawel</creatorcontrib><creatorcontrib>Lewandowski, Michal</creatorcontrib><creatorcontrib>Farkowski, Michal M</creatorcontrib><creatorcontrib>Borowiec, Anna</creatorcontrib><creatorcontrib>Chwyczko, Tomasz</creatorcontrib><creatorcontrib>Pytkowski, Mariusz</creatorcontrib><creatorcontrib>Szwed, Hanna</creatorcontrib><creatorcontrib>Sterlinski, Maciej</creatorcontrib><title>Comparison of the rhythm control treatment strategy versus the rate control strategy in patients with permanent or long-standing persistent atrial fibrillation and heart failure treated with cardiac resynchronization therapy - a pilot study of Cardiac Resynchronization in Atrial Fibrillation Trial (Pilot-CRAfT): study protocol for a randomized controlled trial</title><title>Trials</title><addtitle>Trials</addtitle><description>The only subgroups of patients with heart failure and atrial fibrillation in which the efficacy of cardiac resynchronization therapy has been scientifically proven are patients with indications for right ventricular pacing and patients after atrioventricular junction ablation. However it is unlikely that atrioventricular junction ablation would be a standard procedure in the majority of the heart failure patients with cardiac resynchronization therapy and concomitant atrial fibrillation due to the irreversible character of the procedure and a spontaneous sinus rhythm resumption that occurs in about 10% of these patients.
Pilot-CRAfT is the first randomized controlled trial evaluating the efficacy of a rhythm control strategy in atrial fibrillation patients with cardiac resynchronization therapy devices. The aim of this prospective, single center randomized controlled pilot study is to answer the question whether the patients with cardiac resynchronization therapy and permanent atrial fibrillation would benefit from a strategy to restore and maintain sinus rhythm (that is 'rhythm control' strategy) in comparison to rate control strategy. The study population consists of 60 patients with heart failure and concomitant long-standing persistent or permanent atrial fibrillation who underwent a cardiac resynchronization therapy device implantation at least 3 months before qualification. Study participants are randomly assigned to the rhythm control strategy (including electrical cardioversion and pharmacotherapy) or to the rate control group whose goal is to control ventricular rate. The follow-up time is 12 months. The primary endpoint is the ratio of effectively captured biventricular beats. The secondary endpoints include peak oxygen consumption, six-minute walk test distance, heart failure symptom escalation, reverse remodelling of the heart on echo and quality of life.
NCT01850277 registered on 22 April 2013 (ClinicalTrials.gov).</description><subject>Anti-Arrhythmia Agents - adverse effects</subject><subject>Anti-Arrhythmia Agents - therapeutic use</subject><subject>Atrial Fibrillation - diagnosis</subject><subject>Atrial Fibrillation - physiopathology</subject><subject>Atrial Fibrillation - therapy</subject><subject>Cardiac Resynchronization Therapy - adverse effects</subject><subject>Catheter Ablation - adverse effects</subject><subject>Clinical Protocols</subject><subject>Combined Modality Therapy</subject><subject>Comparative analysis</subject><subject>Defibrillators</subject><subject>Electric Countershock - adverse effects</subject><subject>Electric Countershock - instrumentation</subject><subject>Heart Failure - diagnosis</subject><subject>Heart Failure - physiopathology</subject><subject>Heart Failure - therapy</subject><subject>Humans</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>Pilot Projects</subject><subject>Poland</subject><subject>Prospective Studies</subject><subject>Quality of Life</subject><subject>Recovery of Function</subject><subject>Research Design</subject><subject>Study Protocol</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><issn>1745-6215</issn><issn>1745-6215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp1k92L1DAUxaso7rr67pMEfNGHrm3TTx-EobgqLCjL-Fxu02SaJU1Kklnp_vXebscygysNNNx7zo-TSxIEb-LoMo7L_GNcpFmYJ3EW4qJl_jQ4X0vPjvZnwUvnbqMopRVNXwRnSZaUcVJk509uazOMYKUzmhhBfM-J7SffD4QZ7a1RxFsOfuDaE-cteL6byB23bu8WMVZW6SqQmozgJZoc-S19T0ZuB9AzxFiijN6FzoPupN7NLSedn3vgrQRFhGytVAoBGApVpOdgPREg1d7yJRDvFjAD20lgxHI3adZbo-X9YsR0FsaJhATIKJWZ8--7aT5lfTDd_GPC4JslxNVxiO1D6f3PGRPWNxux_fDpgBut8Ybh4QWeDHAeujODvMd8h6ko3D4gXwXPBSjHXx_-F8Gvqy_b-lt4_ePr93pzHbZZRX3YsiQXFZS0Y1UlWpEI4HFOi0wkNM44T9NStHlBqwySudExEKKNirSMREuB0Yvg88Id9-3AO4aTtaCa0coB7NQYkM1pR8u-2Zm7Jk1KGscFAuoF0ErzH8Bph5mhme9aM9-1BhdeRaS8Wyg7ULyRWhjUskE61myyNMrLjNIEVZePqPDr-CBxglxIrJ8YosXArHHOcrHmiqNmfhSPJXl7PJDV8PcV0D9r9BWN</recordid><startdate>20141004</startdate><enddate>20141004</enddate><creator>Ciszewski, Jan</creator><creator>Maciag, Aleksander</creator><creator>Kowalik, Ilona</creator><creator>Syska, Pawel</creator><creator>Lewandowski, Michal</creator><creator>Farkowski, Michal M</creator><creator>Borowiec, Anna</creator><creator>Chwyczko, Tomasz</creator><creator>Pytkowski, Mariusz</creator><creator>Szwed, Hanna</creator><creator>Sterlinski, Maciej</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20141004</creationdate><title>Comparison of the rhythm control treatment strategy versus the rate control strategy in patients with permanent or long-standing persistent atrial fibrillation and heart failure treated with cardiac resynchronization therapy - a pilot study of Cardiac Resynchronization in Atrial Fibrillation Trial (Pilot-CRAfT): study protocol for a randomized controlled trial</title><author>Ciszewski, Jan ; Maciag, Aleksander ; Kowalik, Ilona ; Syska, Pawel ; Lewandowski, Michal ; Farkowski, Michal M ; Borowiec, Anna ; Chwyczko, Tomasz ; Pytkowski, Mariusz ; Szwed, Hanna ; Sterlinski, Maciej</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b593t-bc26f9a83dc99fbf2fae16375f2315ee448fb67395a2e163dcaffb07480fb3ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Anti-Arrhythmia Agents - adverse effects</topic><topic>Anti-Arrhythmia Agents - therapeutic use</topic><topic>Atrial Fibrillation - diagnosis</topic><topic>Atrial Fibrillation - physiopathology</topic><topic>Atrial Fibrillation - therapy</topic><topic>Cardiac Resynchronization Therapy - adverse effects</topic><topic>Catheter Ablation - adverse effects</topic><topic>Clinical Protocols</topic><topic>Combined Modality Therapy</topic><topic>Comparative analysis</topic><topic>Defibrillators</topic><topic>Electric Countershock - adverse effects</topic><topic>Electric Countershock - instrumentation</topic><topic>Heart Failure - diagnosis</topic><topic>Heart Failure - physiopathology</topic><topic>Heart Failure - therapy</topic><topic>Humans</topic><topic>Medical research</topic><topic>Medicine, Experimental</topic><topic>Pilot Projects</topic><topic>Poland</topic><topic>Prospective Studies</topic><topic>Quality of Life</topic><topic>Recovery of Function</topic><topic>Research Design</topic><topic>Study Protocol</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ciszewski, Jan</creatorcontrib><creatorcontrib>Maciag, Aleksander</creatorcontrib><creatorcontrib>Kowalik, Ilona</creatorcontrib><creatorcontrib>Syska, Pawel</creatorcontrib><creatorcontrib>Lewandowski, Michal</creatorcontrib><creatorcontrib>Farkowski, Michal M</creatorcontrib><creatorcontrib>Borowiec, Anna</creatorcontrib><creatorcontrib>Chwyczko, Tomasz</creatorcontrib><creatorcontrib>Pytkowski, Mariusz</creatorcontrib><creatorcontrib>Szwed, Hanna</creatorcontrib><creatorcontrib>Sterlinski, Maciej</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Trials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ciszewski, Jan</au><au>Maciag, Aleksander</au><au>Kowalik, Ilona</au><au>Syska, Pawel</au><au>Lewandowski, Michal</au><au>Farkowski, Michal M</au><au>Borowiec, Anna</au><au>Chwyczko, Tomasz</au><au>Pytkowski, Mariusz</au><au>Szwed, Hanna</au><au>Sterlinski, Maciej</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of the rhythm control treatment strategy versus the rate control strategy in patients with permanent or long-standing persistent atrial fibrillation and heart failure treated with cardiac resynchronization therapy - a pilot study of Cardiac Resynchronization in Atrial Fibrillation Trial (Pilot-CRAfT): study protocol for a randomized controlled trial</atitle><jtitle>Trials</jtitle><addtitle>Trials</addtitle><date>2014-10-04</date><risdate>2014</risdate><volume>15</volume><issue>1</issue><spage>386</spage><epage>386</epage><pages>386-386</pages><artnum>386</artnum><issn>1745-6215</issn><eissn>1745-6215</eissn><abstract>The only subgroups of patients with heart failure and atrial fibrillation in which the efficacy of cardiac resynchronization therapy has been scientifically proven are patients with indications for right ventricular pacing and patients after atrioventricular junction ablation. However it is unlikely that atrioventricular junction ablation would be a standard procedure in the majority of the heart failure patients with cardiac resynchronization therapy and concomitant atrial fibrillation due to the irreversible character of the procedure and a spontaneous sinus rhythm resumption that occurs in about 10% of these patients.
Pilot-CRAfT is the first randomized controlled trial evaluating the efficacy of a rhythm control strategy in atrial fibrillation patients with cardiac resynchronization therapy devices. The aim of this prospective, single center randomized controlled pilot study is to answer the question whether the patients with cardiac resynchronization therapy and permanent atrial fibrillation would benefit from a strategy to restore and maintain sinus rhythm (that is 'rhythm control' strategy) in comparison to rate control strategy. The study population consists of 60 patients with heart failure and concomitant long-standing persistent or permanent atrial fibrillation who underwent a cardiac resynchronization therapy device implantation at least 3 months before qualification. Study participants are randomly assigned to the rhythm control strategy (including electrical cardioversion and pharmacotherapy) or to the rate control group whose goal is to control ventricular rate. The follow-up time is 12 months. The primary endpoint is the ratio of effectively captured biventricular beats. The secondary endpoints include peak oxygen consumption, six-minute walk test distance, heart failure symptom escalation, reverse remodelling of the heart on echo and quality of life.
NCT01850277 registered on 22 April 2013 (ClinicalTrials.gov).</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>25281275</pmid><doi>10.1186/1745-6215-15-386</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anti-Arrhythmia Agents - adverse effects Anti-Arrhythmia Agents - therapeutic use Atrial Fibrillation - diagnosis Atrial Fibrillation - physiopathology Atrial Fibrillation - therapy Cardiac Resynchronization Therapy - adverse effects Catheter Ablation - adverse effects Clinical Protocols Combined Modality Therapy Comparative analysis Defibrillators Electric Countershock - adverse effects Electric Countershock - instrumentation Heart Failure - diagnosis Heart Failure - physiopathology Heart Failure - therapy Humans Medical research Medicine, Experimental Pilot Projects Poland Prospective Studies Quality of Life Recovery of Function Research Design Study Protocol Time Factors Treatment Outcome |
title | Comparison of the rhythm control treatment strategy versus the rate control strategy in patients with permanent or long-standing persistent atrial fibrillation and heart failure treated with cardiac resynchronization therapy - a pilot study of Cardiac Resynchronization in Atrial Fibrillation Trial (Pilot-CRAfT): study protocol for a randomized controlled trial |
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