[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Regional Cardiology Center, The Copper Health Centre (MCZ),\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":123},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,47,74,100],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":22,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100550751","lower-silesian-orbital-atherectomy-registry-loar-100550751",false,"NCT06451146","Lower Silesian Orbital Atherectomy Registry (LOAR)","Evaluation of the Safety and Efficacy of Orbital Atherectomy (OA) for Calcified Lesions in Patients With Coronary Artery Disease: The Lower Silesian Orbital Atherectomy Registry (LOAR)","LOAR","Inclusion Criteria:\n\n* The presence of moderately to severely calcified lesions.\n\nExclusion Criteria:\n\n* Lack of patient consent\n* Target vessel perforation due to previous unsuccessful lesion preparation\n* Pregnancy","ALL","18 Years",{"count":20,"type":21},500,"ESTIMATED","5 Years","OBSERVATIONAL","The Lower Silesian Orbital Atherectomy Registry (LOAR), is an observational registry collecting all consecutive cases of percutaneous coronary intervention (PCI) performed with the support of the Orbital Atherectomy Device due to the presence of calcified lesion in coronary arteries. Data will be collected in two cooperating cardiac centers (Department of Cardiology, The Copper Health Center, Lubin, Poland, and Department of Cardiology, Provincial Specialized Hospital in Legnica, Poland).",[26,27],"Safety Issues","Efficacy, Self",[29,30,31,32,33],"Percutaneous coronary interventions","Calcified Lesion","Coronary artery diseases","Orbital Atherectomy","Lesion preparation","RECRUITING","2024-08-19",{"date":37,"type":38},"2024-08-21","ACTUAL",{"date":40,"type":38},"2022-05-01",{"date":42,"type":21},"2027-05-01",{"name":44,"class":45},"Regional Cardiology Center, The Copper Health Centre (MCZ),","OTHER",2,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":57,"conditions":58,"keywords":59,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":46},"100537917","lower-silesia-culotte-bifurcation-registry-lscbr-100537917","NCT06284057","Lower Silesia Culotte Bifurcation Registry (LSCBR).","Double Kissing (DK) vs Culotte Culotte. Lower Silesia Culotte Bifurcation Registry (LSCBR).","LSCBR","Inclusion Criteria:\n\n* Presence of significant changes in the coronary bifurcation requiring the implantation of two coronary stents using the Culotte or DK Culotte technique.\n\nExclusion Criteria:\n\n* Patients who underwent PCI with coronary stents prior to the index procedure for the bifurcation lesion studied.",{"count":56,"type":21},400,"The study aimed to evaluate the outcomes of bifurcation PCI using two techniques (Culotte vs. DK-Culotte) using data from a retrospective analysis.",[26,27],[60,61,62,63,64,65],"Percutaneous coronary intervention (PCI)","Bifurcation lesion","Culotte Technique","Double Kiss Culotte Technique","Acute Coronary Syndrome","Two-Stent Technique","2024-03-03",{"date":68,"type":38},"2024-03-06",{"date":70,"type":38},"2013-04-01",{"date":72,"type":21},"2028-04-01",{"name":44,"class":45},{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":79,"acronym":80,"eligibilityCriteria":81,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":82,"targetDuration":22,"studyType":23,"phases":4,"briefSummary":84,"conditions":85,"keywords":86,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":46},"100538233","lower-silesia-sinus-reducer-registry-100538233","NCT06288165","Lower Silesia Sinus Reducer Registry","Coronary Sinus Reducer Implantation for Refractory Angina - Long-Term Evaluation of Device Safety and Efficacy- Lower Silesia Sinus Reducer Registry (LSSRR)","LSSRR","Inclusion Criteria:\n\n1. present of chronic disabling refractory angina pectoris (Canadian Cardiovascular Society \\[CCS\\] classes 2-4) despite maximally tolerated anti-angina medical therapy\n2. Heart team evaluation with consideration of ineligibility for percutaneous or surgical revascularization procedures.\n\nExclusion Criteria:\n\n1. recent acute coronary syndrome (\\\u003C3 months),\n2. recent coronary revascularization (\\\u003C3 months)\n3. a mean right atrial pressure higher than 15 mm Hg\n4. coronary sinus proximal diameter \\\u003C10mm and \\>14mm\n5. life expectancy under 12 months,\n6. advanced heart failure (New York Heart Association \\[NYHA\\] Classification - classes 3-4),\n7. potential implantable cardiac resynchronization therapy defibrillator (CRT-D) implantation candidate.",{"count":83,"type":21},200,"Lower Silesia Sinus Reducer Registry is a , single-center, single-arm registry including patients with chronic disabling refractory angina pectoris (Canadian Cardiovascular Society \\[CCS\\] classes 2-4) despite maximally tolerated anti-angina medical therapy who underwent Coronary Sinus Reducer implantation .",[26,27],[87,88,89,90,91],"Coronary Sinus Reducer","Refractory angina","Chronic coronary artery diseases (CAD)","Non-obstructive Coronary artery diseases (CAD)","Coronary microvascular dysfunction","2024-02-24",{"date":94,"type":38},"2024-03-01",{"date":96,"type":38},"2022-05-11",{"date":98,"type":21},"2027-05-11",{"name":44,"class":45},{"id":101,"slug":102,"hasResults":11,"nctId":103,"briefTitle":104,"officialTitle":105,"acronym":106,"eligibilityCriteria":107,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":108,"enrollmentInfo":109,"targetDuration":22,"studyType":23,"phases":4,"briefSummary":110,"conditions":111,"keywords":112,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":117,"lastUpdatePostDateStruct":118,"startDateStruct":120,"completionDateStruct":121,"leadSponsor":122,"locationsCount":46},"100509704","the-lower-silesia-shockwave-registry-100509704","NCT05916898","The Lower Silesia Shockwave Registry","Evaluation of the Safety and Efficiency of ShockWave Intravascular Lithotripsy (S-IVL) in Coronary Artery Diseases. The Lower Silesia Shockwave Registry (LSSR)","LSSR","Inclusion Criteria:\n\n* The presence of moderately to severely calcified lesions.\n* The presence of significant under-expansion (greater than 20% of the diameter) of the previously implanted stent.\n* Initial failure of the lesion preparation with either the NC balloon catheter or the atherectomy device.\n\nExclusion Criteria:\n\n* Lack of patient consent\n* Target vessel dissection type 3 or higher according to spontaneous coronary artery dissection (SCAD) classification\n* Target vessel perforation due to previous unsuccessful lesion preparation\n* Pregnancy","99 Years",{"count":56,"type":21},"Lower Silesia Shockwave Registry (LSSR), is a observational registry collecting all consecutive cases of percutaneous coronary intervention (PCI) performed with the support of shockwave intravascular lithotripsy in two cooperating cardiac centers (Department of Cardiology, The Copper Health Centre, Lubin Poland, and Department of Cardiology, Provincial Specialized Hospital in Legnica, Poland).",[26,27],[29,30,113,114,31,115,116],"Shockwave intravascular lithotripsy","Stent under-expansion","lesion preparation","stent optimalization","2023-06-21",{"date":119,"type":38},"2023-06-23",{"date":40,"type":38},{"date":42,"type":21},{"name":44,"class":45},""]