[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"stent-graft-stenosis\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:stent-graft-stenosis":33},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,49],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100458054","copenhagen-mesenteric-stent-study---a-randomized-trial-of-stent-versus-covered-stent-treatment-for-chronic-mesenteric-ischemia-100458054",false,"NCT05244629","Copenhagen Mesenteric Stent Study - A Randomized Trial of Stent Versus Covered Stent Treatment for Chronic Mesenteric Ischemia","COMESS","Inclusion Criteria:\n\n* Patients with symptomatic CMI of atherosclerotic or atherothrombotic etiology\n* Intended endovascular treatment\n* Symptoms consistent with CMI (pain, weight loss, diarrhea)\n* Significant ostial stenosis (\\>50%) of the superior mesenteric artery on CTA\n* Significant stenosis on angiography (\\>50% or \\>15mmHg pressure gradient)\n* Patients \\> 18 years\n\nExclusion Criteria:\n\n* No informed consent\n* Non atherosclerotic cause of MI\n* Acute mesenteric ischemia (AMI)\n* Signs of acute bowel ischemia, peritonitis, laparotomy, sepsis\n* Previous stent treatment in the superior mesenteric artery(ies)\n* Target artery lesions \\>4cm in length\n* Unable to cross lesion with guidewire\n* Non-significant stenosis angiographically\n* Pregnancy\n* Allergies to contrast media or stent materials","ALL","18 Years",{"count":19,"type":20},98,"ESTIMATED","INTERVENTIONAL",[23],"NA","Chronic mesenteric ischemia (CMI) is often caused by narrowings in the arteries providing blood to the intestines. Endovascular stent placement is considered the preferred treatment for this condition. Guidelines increasingly support the use of so called covered stents (CS) in stead of bare stents (BMS) for this use but the level of evidence for this is limited. Using CS incur additional costs for healthcare short-term but may prevent recurrence of narrowing and symptoms postoperatively benefitting patients and healthcare.\n\nStudy Objective:\n\nTo evaluate the outcomes after stenting of mesenteric arteries using BMS or CS.\n\nStudy Outcome:\n\nPrimary stent patency 1 year after placement\n\nThe trial will also evaluate complications, how often stents need to be reoperated, Quality of Life (QoL) and reasons for subjects death\n\nMethod:\n\nThis is a so called prospective, randomized controlled trial comparing CS vs. BMS. This means that one patients have agrred to treatment they will be randomly selected for treatment with either CS or BMS . The stent metal structure is identical in the two implants and the only difference is the graft covering, making this study unique.\n\nThe study will also collect blood samples for a biobank that will be used to study markers of disease and how these effect treatment outcomes.\n\nAll patients referred to the Department of Vascular Surgery due to CMI are considered for inclusion if they havechronic symptoms consistent with CMI, significant stenosis or occlusion of the superior mesenteric artery and are \\> 18 years Subjects not able to provide informed consent or who have non atherosclerotic cause of CMI, signs of acute loss of blood flow to the intestines cannot participate. Previous stent treatment in the superior mesenteric artery, pregnancy, allergies to contrast or stent materials are also reasons for not being included in this trial.\n\nSide effects, risks and disadvantages for participants The risk for procedure-related complications is less than 5% and similar in both study groups. Most short-term complications are related to vascular access sites and consist of local bleeding and thrombosis. Other potential complications include impaired renal function due to contrast use, contrast allergy, arterial dissection and death.",[26,27,28,29,30,31,32,33,34,35],"Mesenteric Ischemia","Bowel; Ischemic","Superior Mesenteric Atherosclerosis","Mesenteric Artery Stenosis","Stent Restenosis","Stent Occlusion","Stent Thrombosis","Stent-Graft Stenosis","Stent-Graft Thrombosis","Stent-Graft Restenosis","RECRUITING","2023-06-09",{"date":39,"type":40},"2023-06-12","ACTUAL",{"date":42,"type":20},"2023-06",{"date":44,"type":20},"2029-08",{"name":46,"class":47},"Rigshospitalet, Denmark","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":55,"enrollmentInfo":56,"targetDuration":58,"studyType":59,"phases":4,"briefSummary":60,"conditions":61,"keywords":69,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":74,"lastUpdatePostDateStruct":75,"startDateStruct":77,"completionDateStruct":79,"leadSponsor":81,"locationsCount":48},"100463055","endobarc-s-study-endovascular-branched-stent-grafts-for-aortic-arch-pathologies-in-spain-100463055","NCT05309707","ENDOBARC-S Study: \"Endovascular Branched Stent-grafts for Aortic ARCh Pathologies in Spain\"","Inclusion Criteria:\n\n* Patient is between 18 and 90 years old\n* Patient with aortic arch pathologies (aneurysm, pseudoaneurysm, dissection, penetrating ulcer, intramural hematoma), treated by branched stent-grafts (Nexus stent graft system©, Relay® Branch or Zenith arch branch graft®, with proximal landing at zone 0.\n* Patient must be available for the appropriate follow-up times for the duration of the study\n* Informed consent signed.\n\nExclusion Criteria:\n\n* Patient less than 18 years old or more than 90 years old.\n* Patient has allergies to materials necessary for endovascular repair (e.g. contrast media, anticoagulants or heparin, nitinol, polyester, gold, platinum-iridium)\n* Patient has systemic infection or suspected systemic infection\n* Patient has thrombocytopenia (platelet count \\\u003C 150000\u002Fµl)\n* Patient has untreated hyperthyroidism\n* Patient has a progressive or untreated malignancy.\n* Patient is pregnant or breastfeeding.\n* Patient has a life expectancy of less than 1 year.\n* Not informed consent signed","90 Years",{"count":57,"type":20},100,"5 Years","OBSERVATIONAL","The ENDOBARC-S post-market clinical follow-up study is undertaken to evaluate the prevention of death related to aortic arch pathologies when treated by branch stent graft systems (Nexus stent-graft system®, Relay Branch® or Zenith arch branch graft®), with proximal landing at zone 0.\n\nThe secondary objective is to evaluate the safety and clinical performance of the studied devices.",[62,63,64,33,65,66,67,68],"Thoracic Aortic Aneurysm","Thoracic Aortic Dissection","Stent-Graft Endoleak","Intramural Hematoma","Aortic Diseases","Cardiovascular Diseases","Vascular Diseases",[70,71,72,73],"Aorta","Thoracic aortic aneurysm","Thoracic aorta dissection","Endovascular repair","2022-03-24",{"date":76,"type":40},"2022-04-04",{"date":78,"type":40},"2022-01-01",{"date":80,"type":20},"2027-12-31",{"name":82,"class":83},"Vascular Investigation Network Spanish Society for Angiology and Vascular Surgery","NETWORK"]