[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Bochang\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":43},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":4},"100526884","clinical-trial-of-biolimus-coated-intracranial-balloon-dilation-catheter-100526884",false,"NCT06140550","Clinical Trial of Biolimus-coated Intracranial Balloon Dilation Catheter","Prospective, Multicenter, Randomized Controlled Clinical Trial to Evaluate the Effectiveness and Safety of Biolimus-coated Intracranial Balloon Dilation Catheter Treatment of Patients With Symptomatic Intracranial Atherosclerotic Stenosis","Inclusion Criteria:\n\n* 18 to 80 years old;\n* Symptomatic intracranial artery stenosis, and the degree of visual stenosis of target blood vessels under intracranial angiography is 70\\~99%(WASID method);\n\nExclusion Criteria:\n\n* Target blood vessels are seriously calcified and distorted, and it is difficult to put the interventional instruments in place or recover;\n* Ischemic cerebral infarction occurred 3 weeks before surgery;\n* Cerebral hemorrhage 3 months before operation;","ALL","18 Years","80 Years",{"count":20,"type":21},204,"ESTIMATED","INTERVENTIONAL",[24],"NA","This test took the target lesion restenosis rate 6 months after the operation as the main endpoint to verify the effectiveness of the intracranial balloon expansion catheter of Biolimus coating. After completing the follow-up 6 months after the operation, a clinical summary report was issued for the registration application of the product, and on this basis, 12 months of postoperative follow-up was carried out to evaluate the mid-term curative effect.",[27],"Intracranial Atherosclerotic Stenosis",[29,30],"Intracranial balloon","stenosis","NOT_YET_RECRUITING","2023-11-17",{"date":34,"type":35},"2023-11-20","ACTUAL",{"date":37,"type":21},"2023-11",{"date":39,"type":21},"2026-12",{"name":41,"class":42},"Bochang","INDUSTRY",""]