[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100558674":3},{"organization":4,"armGroups":7,"interventions":8,"overallOfficials":7,"centralContacts":13,"locations":23,"responsibleParty":40,"collaborators":7,"id":42,"slug":43,"hasResults":44,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":7,"eligibilityCriteria":48,"healthyVolunteers":44,"sex":49,"minAge":50,"maxAge":51,"enrollmentInfo":52,"targetDuration":7,"studyType":55,"phases":7,"briefSummary":56,"conditions":57,"keywords":7,"overallStatus":26,"whyStopped":7,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":65,"completionDateStruct":66,"leadSponsor":68,"locationsCount":69},{"fullName":5,"class":6},"The First Affiliated Hospital of Soochow University","OTHER",null,[9],{"type":10,"name":11,"description":12,"armGroupLabels":7,"otherNames":7},"DIAGNOSTIC_TEST","CMV\u002FEBV-CMI","The CMV\u002FEBV-CMI is tested before conditioning regimen and 30 days, 45 days, 60 days, 90 days, 120 days, 180 days after transplantation.",[14,19],{"name":15,"role":16,"phone":17,"phoneExt":7,"email":18},"Feng Chen, PhD","CONTACT","13584861215","13584861215@163.com",{"name":20,"role":16,"phone":21,"phoneExt":7,"email":22},"Depei Wu, PhD","67781856","drwudepei@163.com",[24],{"facility":25,"status":26,"city":27,"state":28,"zip":29,"country":30,"countryCode":31,"cosmosGeoPoint":32,"geoPoint":37,"contacts":38},"First Affiliated Hospital of Soochow University","RECRUITING","Suzhou","Jiangsu","215006","China","CN",{"type":33,"coordinates":34},"Point",[35,36],120.59538,31.30408,{"lat":36,"lon":35},[39],{"name":15,"role":16,"phone":17,"phoneExt":7,"email":18},{"type":41,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR","100558674","evaluation-of-cmvebv-cmi-in-haploid-hsct-100558674",false,"NCT06554197","Evaluation of CMV\u002FEBV-CMI in Haploid HSCT","Evaluation of Cytomegalovirus and Epstein-Barr Virus Specific Immune Reformulation in Prophylaxis for Cytomegalovirus in Haploid Hematopoietic Stem Cell Transplantation","Inclusion Criteria:\n\n1. All patients were diagnosed with hemopathy.\n2. All patients should have the indication of Haploidentical hematopoietic stem cell transplant and receive the prophylaxis for cytomegalovirus.\n3. All patients should sign an informed consent document indicating that they understand the purpose of and procedures required for the study and be willing to participate in the study.\n\nExclusion Criteria:\n\nPatients with any conditions not suitable for the trial (investigators' decision).","ALL","16 Years","60 Years",{"count":53,"type":54},60,"ESTIMATED","OBSERVATIONAL","The purpose of this prospective, open-label, Single Arm, single-center study is to evaluate the cytomegalovirus and Epstein-Barr virus specific immune reestablishment for patients with hemopathy undergoingin prophylaxis for cytomegalovirus in haploid hematopoietic stem cell transplantation(haplo-HSCT) .",[58,59,60],"Hematopoietic Stem Cell Transplantation","Cytomegalovirus Infections","Epstein-Barr Virus Infections","2024-08-13",{"date":63,"type":64},"2024-08-15","ACTUAL",{"date":61,"type":54},{"date":67,"type":54},"2026-07-31",{"name":5,"class":6},1]