{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","value":"1"}]}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"2"},{"groupId":"OG001","value":"0"}],"units":"Participants"}],"groups":[{"description":"Patients receiving umbilical cord blood for hematopoietic rescue following myeloablative conditioning.","id":"OG000","title":"Myeloablative Conditioning"},{"description":"Patients receiving umbilical cord blood for hematopoietic rescue following non-myeloablative conditioning","id":"OG001","title":"Reduced Intensity Conditioning"}],"paramType":"NUMBER","populationDescription":"No subject receiving reduced intensity conditioning was evaluable for the event of chronic GVHD (0/3 subjects survived to day +100)","reportingStatus":"POSTED","timeFrame":"After Day +100","title":"Incidence of Chronic GVHD","type":"SECONDARY","unitOfMeasure":"participants"}