[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Albert Schweitzer Ziekenhuis, Netherlands\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":65},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,40],{"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":21,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":39},"100586760","optimal-stent-deployment-strategy-of-contemporary-stents---registry-to-evaluate-percutaneous-coronary-intervention-using-bioresorbable-scaffolds-with-thinner-strut-construction-and-guidance-by-intracoronary-imaging-to-reduce-scaffold-failure-100586760",false,"NCT06919562","OPtimal stEnt Deployment stRategy oF Contemporary sTents - Registry to Evaluate Percutaneous Coronary Intervention Using Bioresorbable Scaffolds With Thinner-strut Construction and Guidance by intracOronary Imaging to REduce Scaffold Failure","PERFECTRESTORE","Inclusion Criteria:\n\n1. Stable coronary artery disease with one or more significant epicardial stenosis in native coronary arteries suitable for OCT or IVUS-guided PCI with BRS implantation.\n2. Subject must be at least 18 years of age\n3. Written consent to participate in the study\n\nExclusion Criteria:\n\n1. Culprit lesions in the setting of acute coronary syndrome.\n2. Lesions with severe calcification.\n3. Lesions in a coronary artery with severe tortuosity.\n4. Left main coronary artery lesions.\n5. Bifurcation lesions.\n6. Ostial lesions.\n7. Lesions with a difference in proximal and distal reference diameter of \\>0.5 mm by visual judgement of the coronary angiogram by the treating operator.\n8. Treatment of in-stent restenosis or stent thrombosis.\n9. History of definite stent thrombosis.\n10. Lesions in coronary artery bypass grafts.\n11. Lesions not suitable for OCT or IVUS catheter delivery and imaging, e.g. due to tortuosity or distal localisation.\n12. Creatinine Clearance ≤ 30 ml\u002Fmin\u002F1.73 m2 as calculated by MDRD formula for estimated GFR.\n13. Contraindication to dual antiplatelet therapy with aspirin and a P2Y12 inhibitor or (if indicated) NOAC and P2Y12 inhibitor.\n14. Planned non-deferrable major surgery after PCI.\n15. Known comorbidity associated with a life expectancy \\\u003C1 year.\n16. Unable to understand and follow study-related instructions or unable to comply with study protocol.","ALL","18 Years",{"count":19,"type":20},117,"ESTIMATED","3 Years","OBSERVATIONAL","Implantation of a metallic drug-eluting stent (DES) is currently the gold standard in percutaneous coronary intervention (PCI). However, a DES has several limitations on the long-term, such as chronic local inflammation which may lead to in-stent restenosis, absence of physiological coronary vasomotion and vessel caging which makes future coronary artery bypass grafting (CABG) impossible. A bioresorbable scaffold (BRS) is designed to overcome these limitations. The first generation BRS was shown to be clinically inferior to DES due to a slightly higher rate of stent thrombosis. To overcome this problem, several scientific developments have been achieved in the past few years, such as thinner BRS strut construction and improved implantation technique by using PSP (predilatation, sizing, postdilatation) method and intracoronary imaging guidance with optical coherence tomography (OCT) or intravasculair ultrasound (IVUS). A PCI protocol that combines implantation of a second generation thin-strut BRS, mandatory PSP implantation method and mandatory intracoronary imaging-guidance has not yet been investigated. The aim of this study is to investigate feasibility of a new PCI protocol with implantation of the second generation Meres100 thin-strut BRS combined with a protocolized PSP implantation technique guided by intracoronary imaging.",[25,26],"Coronary Arterial Disease (CAD)","Percutaneous Coronary Intervention (PCI)","RECRUITING","2026-05-15",{"date":30,"type":31},"2026-05-18","ACTUAL",{"date":33,"type":31},"2025-11-04",{"date":35,"type":20},"2030-08",{"name":37,"class":38},"Albert Schweitzer Ziekenhuis, Netherlands","OTHER",1,{"id":41,"slug":42,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":44,"acronym":45,"eligibilityCriteria":46,"healthyVolunteers":11,"sex":16,"minAge":47,"maxAge":4,"enrollmentInfo":48,"targetDuration":50,"studyType":22,"phases":4,"briefSummary":51,"conditions":52,"keywords":54,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":39},"100568595","bascom-cleft-lift-for-primary-wound-healing-in-complex-and-recurrent-sacrococcygeal-pilonidal-sinus-disease-100568595","NCT06683274","Bascom Cleft Lift for Primary Wound Healing in Complex and Recurrent Sacrococcygeal Pilonidal Sinus Disease","BATCRAC","Inclusion Criteria:\n\n* 16 years of age and older\n* Symptomatic complex or recurrent pilonidal sinus disease\n* Planned for surgical treatment\n* Signed informed consent\n\nExclusion Criteria:\n\n* Pregnant\n* Insufficient understanding of the Dutch language or otherwise unable to give consent","16 Years",{"count":49,"type":20},58,"6 Months","The goal of this observational study is to improve care for patients with complex or recurrent pilonidal sinus disease by developing and implementing a best practice care pathway, including a standardized cleft lift operation.\n\nThe main question it aims to answer is: Does a best practice care pathway with standardized cleft lift operation lead to shorter wound healing time and time to return to normal activities, compared to current standard care, with traditional excision techniques.",[53],"Pilonidal Sinus",[55,56],"Pilonidal sinus","Bascom cleft lift","2025-09-29",{"date":59,"type":31},"2025-09-30",{"date":61,"type":31},"2025-02-20",{"date":63,"type":20},"2027-04",{"name":37,"class":38},""]