[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100563227":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":21,"centralContacts":26,"locations":31,"responsibleParty":48,"collaborators":20,"id":50,"slug":51,"hasResults":52,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":20,"eligibilityCriteria":56,"healthyVolunteers":57,"sex":58,"minAge":59,"maxAge":60,"enrollmentInfo":61,"targetDuration":20,"studyType":64,"phases":65,"briefSummary":67,"conditions":68,"keywords":20,"overallStatus":34,"whyStopped":20,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":79},{"fullName":5,"class":6},"The General Hospital of Western Theater Command","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Experimental group","EXPERIMENTAL","Combined platelet",[13],"Combination Product: Combined platelets",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"COMBINATION_PRODUCT","Combined platelets","1 therapeutic dose combined platelet contained no less than 2.5 ×10\\^11 platelets as a quality standard.",[9],null,[22],{"name":23,"affiliation":24,"role":25},"zhang li","The General Hospital of Weastern Theater Command","PRINCIPAL_INVESTIGATOR",[27],{"name":23,"role":28,"phone":29,"phoneExt":20,"email":30},"CONTACT","+86 13982283001","1062747632@qq.com",[32],{"facility":33,"status":34,"city":35,"state":36,"zip":37,"country":38,"countryCode":39,"cosmosGeoPoint":40,"geoPoint":45,"contacts":46},"Li Zhang","RECRUITING","Chengdu","Sichuan","610083","China","CN",{"type":41,"coordinates":42},"Point",[43,44],104.06667,30.66667,{"lat":44,"lon":43},[47],{"name":23,"role":28,"phone":29,"phoneExt":20,"email":30},{"type":25,"investigatorFullName":23,"investigatorTitle":49,"investigatorAffiliation":5,"oldNameTitle":20,"oldOrganization":20},"PHD，Professor","100563227","phase-4-clinical-study-of-combined-platelet-transfusion-100563227",false,"NCT06613425","Clinical Study of Combined Platelet Transfusion","Combined Platelet Transfusion:A Single-arm, Open, Prospective, Non-inferiority Clinical Trial","Inclusion Criteria:\n\n* 1\\. Aged 18-65 years; 2. Disease treatment in the research hospital; 3. Applied for platelet transfusion therapy.\n\nExclusion Criteria:\n\n* 1\\. One month before the start of this study, he participated in other clinical trials of drugs and instruments related to platelet transfusion efficacy; 2. Without platelet transfusion indications; 3. Only received platelet transfusion in the outpatient department and left the hospital without efficacy evaluation after transfusion; 4. Gave up platelet transfusion therapy for any reason after enrollment; 5. Transferred or discharged from hospital for any reason before platelet transfusion after enrollment; 6. Did not receive combined platelet transfusion during the 6-month treatment period after enrollment",true,"ALL","18 Years","65 Years",{"count":62,"type":63},86,"ESTIMATED","INTERVENTIONAL",[66],"PHASE4","Platelet transfusion is an irreplaceable and important treatment method for clinical prevention and treatment of thrombocytopenia or platelet dysfunction. Due to various factors, it is difficult to achieve platelet ABO complete homotypic transfusion in clinical practice. When ABO-compatible platelets cannot be obtained, plasma-reduced platelets, platelets with low anti-A or anti-B titers are often used in clinical practice to reduce the risk of ABO-incompatible platelet-compatible transfusion reactions. The combined platelets prepared in this study can achieve ABO primary and secondary side compatible infusion.",[69],"Hematologic Diseases","2024-09-23",{"date":72,"type":73},"2024-09-26","ACTUAL",{"date":75,"type":73},"2024-08-01",{"date":77,"type":63},"2025-10-28",{"name":5,"class":6},1]