[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100374065":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":34,"centralContacts":38,"locations":43,"responsibleParty":60,"collaborators":26,"id":63,"slug":64,"hasResults":65,"nctId":66,"briefTitle":67,"officialTitle":68,"acronym":26,"eligibilityCriteria":69,"healthyVolunteers":65,"sex":70,"minAge":71,"maxAge":72,"enrollmentInfo":73,"targetDuration":26,"studyType":76,"phases":77,"briefSummary":79,"conditions":80,"keywords":82,"overallStatus":46,"whyStopped":26,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":88,"completionDateStruct":90,"leadSponsor":92,"locationsCount":93},{"fullName":5,"class":6},"University of Illinois at Chicago","OTHER",[8,15],{"label":9,"type":10,"description":11,"interventionNames":12},"Arm 1","ACTIVE_COMPARATOR","ARM 1 -transdermal granisetron plus intravenous dexamethasone",[13,14],"Drug: Granisetron Transdermal Patch","Drug: Intravenous Dexamethasone",{"label":16,"type":10,"description":17,"interventionNames":18},"ARM 2","ARM 2 -intravenous ondansetron plus intravenous dexamethasone",[14,19],"Drug: Ondansetron",[21,27,30],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DRUG","Granisetron Transdermal Patch","Antiemetic",[9],null,{"type":22,"name":28,"description":24,"armGroupLabels":29,"otherNames":26},"Intravenous Dexamethasone",[16,9],{"type":22,"name":31,"description":32,"armGroupLabels":33,"otherNames":26},"Ondansetron","ondansetron",[16],[35],{"name":36,"affiliation":5,"role":37},"Karen Sweiss, PharmD","PRINCIPAL_INVESTIGATOR",[39],{"name":36,"role":40,"phone":41,"phoneExt":26,"email":42},"CONTACT","312-996-0875","ksweis2@uic.edu",[44],{"facility":45,"status":46,"city":47,"state":48,"zip":49,"country":50,"countryCode":51,"cosmosGeoPoint":52,"geoPoint":57,"contacts":58},"University of Illinois Cancer Center","RECRUITING","Chicago","Illinois","60612","United States","US",{"type":53,"coordinates":54},"Point",[55,56],-87.65005,41.85003,{"lat":56,"lon":55},[59],{"name":36,"role":40,"phone":41,"phoneExt":26,"email":42},{"type":37,"investigatorFullName":61,"investigatorTitle":62,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"Karen Sweiss","Clinical Assistant Professor","100374065","phase-4-bmt-08-a-comparative-effectiveness-study-of-transdermal-granisetron-to-ondansetron-100374065",false,"NCT04150614","BMT-08: A Comparative Effectiveness Study of Transdermal Granisetron to Ondansetron","BMT-08: A Comparative Effectiveness Study of the Efficacy and Safety of Transdermal Granisetron to Ondansetron in the Prevention of Nausea and Vomiting in Patients Undergoing Preparative Chemotherapy and Hematopoietic Stem Cell Transplantation","Inclusion Criteria:\n\n* Age 18-75 years at time of enrollment receiving either a preparative regimen and either an autologous or allogeneic stem cell transplant.\n* No vomiting ≤ 24 hours prior to registration\n* No treatment with an antipsychotic agent such as risperidone, quetiapine, clozapine, phenothiazine or butyrophenone for ≤ 30 days' prior registration or planned during protocol therapy. No patients will be removed from these treatments for study enrollment purposes.\n* No chronic phenothiazine administration as an antipsychotic agent (patients may receive prochlorperazine and other phenothiazines as rescue antiemetic therapy). No patients will be removed from these treatments for study enrollment purposes.\n* No known hypersensitivity to granisetron\n\nExclusion Criteria:\n\n* Concurrent use of amifostine\n* Known hypersensitivity to granisetron patch or ondansetron\n* Patients with a history of long QT syndrome or Torsade de Pointes","ALL","18 Years","75 Years",{"count":74,"type":75},90,"ESTIMATED","INTERVENTIONAL",[78],"PHASE4","Patients undergoing either an autologous or allogeneic hematopoietic stem cell transplant (HSCT) and receiving preparative chemotherapy experience a considerable amount of chemotherapy-induced nausea and vomiting (CINV). Current strategies at reducing CINV in this patient population are suboptimal due to lack of efficacy and supportive evidence, potential for increased adverse events, and drug-drug and drug-disease contraindications.",[81],"Nausea With Vomiting Chemotherapy-Induced",[83],"Hematopoietic Stem Cell Transplantation","2025-11-07",{"date":86,"type":87},"2025-11-12","ACTUAL",{"date":89,"type":87},"2020-05-14",{"date":91,"type":75},"2026-07",{"name":5,"class":6},1]