[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Scitech Produtos Medicos SA\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":73},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,45],{"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":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100630702","brazilian-prospective-registry-of-the-inspiron-evo-drug-eluting-stent-in-complex-coronary-lesions-100630702",false,"NCT07491107","Brazilian Prospective Registry of the Inspiron EVO Drug-Eluting Stent in Complex Coronary Lesions","National Prospective Registry of the Inspiron EVO Drug-Eluting Stent in Complex Coronary Lesions","PCI EVOlution","Inclusion Criteria:\n\n* Individuals aged 18 years or older presenting with complex coronary lesions requiring percutaneous coronary intervention (PCI).\n* Individuals who provide consent and are willing to comply with the follow-up protocol.\n* Individuals who received treatment with the Inspiron™ EVO Stent.\n* Individuals with lesions ≥ 30 mm in length (Subprotocol 1).\n* Individuals with significantly calcified coronary lesions (moderate to severe according to the ACC\u002FAHA classification B1, B2, or C), with or without indication for lesion preparation techniques (Subprotocol 2).\n* Individuals with multivessel coronary artery disease (≥2 affected coronary vessels, with at least one vessel of small diameter ≤2.5 mm) (Subprotocol 3).\n* Individuals included in Subprotocol 1, 2, or 3. The evaluated segment must be accessible to the IVUS (Intravascular Ultrasound) catheter (Subprotocol 4).\n\nExclusion Criteria:\n\n* Lesions in saphenous vein grafts or internal mammary grafts.\n* Contraindication to the use of a drug-eluting stent.\n* Individuals who were treated during the index procedure with any stent other than the Inspiron™ EVO Stent.","ALL","18 Years",{"count":20,"type":21},2000,"ESTIMATED","12 Months","OBSERVATIONAL","The objective is to evaluate the efficacy and safety of the Inspiron™ EVO drug-eluting stent in complex coronary lesions in a real-world population. Patients with symptomatic ischemic heart disease due to lesions in native coronary arteries and restenotic lesions will be treated with the Inspiron™ EVO drug-eluting stent.",[26,27,28,29,30,31],"Coronary Artery Disease (CAD)","Stenosis Coronary","Small Vessel Ischemic Disease","Multivessel Coronary Artery Disease","Calcific Coronary Arteriosclerosis","Complex Coronary Lesions","NOT_YET_RECRUITING","2026-03-24",{"date":35,"type":36},"2026-03-30","ACTUAL",{"date":38,"type":21},"2026-04-30",{"date":40,"type":21},"2030-04-30",{"name":42,"class":43},"Scitech Produtos Medicos SA","INDUSTRY",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":55,"phases":56,"briefSummary":58,"conditions":59,"keywords":4,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":72},"100523473","the-solaris-de-endoprosthesis-for-the-treatment-of-av-access-stenosis-or-occlusion-100523473","NCT06096142","The Solaris DE Endoprosthesis for the Treatment of AV Access Stenosis or Occlusion","Prospective, Randomized, Controlled, Multicenter Study of the Solaris DE Endoprosthesis in the Treatment of Venous Outflow Stenosis or Occlusion in Hemodialysis Patients","DEScover","Inclusion Criteria:\n\n* The participant has a mature AV Fistula (AVF) or Graft (AVG) in the arm created ≥ 30 days before the initial procedure and is in use for dialysis therapy\n* The participant has clinical and\u002For hemodynamic evidence of a venous outflow obstruction or AV fistula or graft dysfunction. The stenotic lesion is ≥ 50%, with a maximum length of 8 cm and a distal reference vessel diameter from 4.0 mm to 9.0 mm\n* The participan provides written informed consent prior to any study-specific procedure\n* The participan is willing to undergo all follow-up evaluations according to the specified schedule over 24 months\n\nAngiographic Inclusion Criteria:\n\n* The target lesion originates ≥ 3 cm from the cannulation segment (needling zone)\n* The target lesion is located:\n\n  1. In one arm (including the cephalic arch) in a participant with AVF, and not in the cannulation segment, OR\n  2. In the anastomosis or juxta-anastomosis in a participant with AVF (a juxta-anastomosis is defined as a location where the stent crosses the venous anastomosis)\n* The target lesion includes a de novo stenotic lesion or restenosis\n* The target lesion is ≥ 5 cm from the arterial anastomosis\n* The target lesion has ≥ 50% stenosis according to the operator's visual judgment\n* The distal reference vessel diameter of the target lesion is between 4.0 mm and 9.0 mm by the operator's visual judgment\n* Single or multiple target lesions measuring ≤ 8 cm in total length by the operator's visual judgment\n* Single or multiple target lesions should be covered by a single stent or multiple overlapping stents, provided they are treated as a single lesion with a maximum length of 8 cm\n* Successful target lesion pre-dilatation is defined as crossover of the guidewir resulting in full expansion of the pre-dilatation balloon\n* The participant has up to 1 (one) non-target lesion in the access circuit requiring intervention in the initial procedure. The non-target lesion must be at least 10 cm away from the target lesion. The non-target lesion can only be treated with standard PTA alone\n* Does not have stent implanted or it has been in the access circuit for ≥ 30 days since placement and patent with ≤ 30% stenosis and located ≥ 5 cm from the target lesion\n* The non-target lesion must be successfully treated at the time of the initial procedure (success measured as ≤30% residual stenosis and no complications).\n\nExclusion Criteria:\n\n* Pregnant, breastfeeding or with intention to become pregnant in the next year\n* The participant has any major endovascular or surgical procedure planned (including in the access circuit) within 30 days of the initial procedure\n* It was not possible to pre-dilate the lesion to be treated with Solaris DE\n* Planned surgical revision of the access site\n* Known or suspected infection of the hemodialysis access site, systemic infection and\u002For sepsis\n* Patients on immunosuppressive therapy\n* Known active coagulopathy or bleeding diathesis\n* Known hypersensitivity to nickel titanium alloy, contrast or sirolimus\n* Contraindication to antiplatelet, anticoagulant or thrombolytic therapies\n* Known allergy to contrast agents or medications administered to perform endovascular intervention that cannot be adequately premedicated\n* Life expectancy of less than 12 months\n* Has a stent or endoprosthesis located anywhere in the AV access circuit that is not patent (\\> 30% stenosis) or implanted \\\u003C 30 days\n* The participant's hemodialysis access is expected to be abandoned within 6 months\n* The participantis is enrolled in another trial involving an investigational product (pharmaceutical, biological or medical device)\n* The patient has a permanent central venous catheter (CVC) for dialysis access, except when its use is temporary, as a bridge to treatment through the access circuit, with a plan for removal after a successful dialysis session after the initial procedure\n\nAngiographic Exclusion Criteria:\n\n* The target lesion is located inside an endoprosthesis\n* Target lesion treatment would involve the cannulation segment (needling zone)\n* The target lesion is \\\u003C 5 cm from the arterial anastomosis\n* There was a dissection or rupture of the treated vessel during the initial treatment that could not be controlled\n* Evidence of an aneurysm, pseudoaneurysm or acute thrombus (i.e. one that has been treated ≤ 15 days) within the target lesion\n* The target lesion is, and\u002For Solaris DE would be placed anywhere:\n\n  1. Through the elbow\n  2. In a region that causes bending of the endoprosthesis or bony protrusion over it\n  3. In the cannulation segment (needling zone)\n  4. Inside any part of a pre-existing stent or endoprosthesis (apart from an access arteriovenous graft)\n  5. Lower extremity\n  6. Non-synthetic graft\n  7. Central thoracic veins located proximal to the cephalic vein arch\n* The target lesion is located in such a way that the insertion of a stent would result in a \"kink\" area that requires a stent bridge between the Solaris DE and an existing stent or stent graft\n* The individual has more than 1 (one) non-target lesion (≥ 50% stenosis) that requires intervention in the initial procedure",{"count":54,"type":21},120,"INTERVENTIONAL",[57],"NA","The goal of this clinical trial is to demonstrate the safety and efficacy of Solaris DE Endoprosthesis in the treatment of stenosis or occlusion within the outflow circuit of the dialysis access including arteriovenous (AV) fistula and synthetic AV graft.\n\nParticipants will be treated with Solaris DE Endoprosthesis. Researchers will compare the treatment with investigational product to Percutaneous Transluminal Angioplasty (PTA) alone within the AV fistula cohort in order to demonstrate superiority of Solaris DE.",[60,61,62],"Venous Stenosis","Venous Occlusion","Chronic Renal Failure","RECRUITING","2026-03-13",{"date":66,"type":36},"2026-03-17",{"date":68,"type":36},"2024-08-30",{"date":70,"type":21},"2028-02",{"name":42,"class":43},5,""]