{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","value":"2"},{"groupId":"OG001","value":"1"}]}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"2"},{"groupId":"OG001","value":"2"}],"units":"Participants"}],"description":"Number of participants with neutrophil engraftment receiving umbilical cord blood for hematopoietic rescue following myeloablative or non-myeloablative conditioning","groups":[{"description":"Patients receiving umbilical cord blood for hematopoietic rescue following myeloablative conditioning.\n\n2/2 evaluable subjects engrafted at +45 and +90 days.","id":"OG000","title":"Myeloablative Conditioning"},{"description":"Patients receiving umbilical cord blood for hematopoietic rescue following non-myeloablative conditioning\n\n1/2 evaluable subjects engrafted at +45 and +90 days.","id":"OG001","title":"Reduced Intensity Conditioning"}],"paramType":"NUMBER","populationDescription":"Only 2 subjects were evaluable from each group at the +45 day mark. The same number were evaluable at the +90 day mark.","reportingStatus":"POSTED","timeFrame":"+45 and 90 days","title":"Number of Participants With Neutrophil Engraftment","type":"PRIMARY","unitOfMeasure":"participants"}