{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","value":"29"}]}],"title":"Successful removal at 21 days"},{"categories":[{"measurements":[{"groupId":"OG000","value":"1"}]}],"title":"Device not effective"}],"denoms":[{"counts":[{"groupId":"OG000","value":"30"}],"units":"Participants"}],"description":"Evaluated by the proportion of Subjects who have had a successful Device placement and developed a functionally adequate anastomosis within 21 days post procedure (i.e. minimal or no extravasation noted during post-placement)","groups":[{"description":"Performance evaluation of the AMS Continuum device in facilitating vesico-urethral anastomosis following a radical prostatectomy","id":"OG000","title":"Continuum Device"}],"paramType":"COUNT_OF_PARTICIPANTS","reportingStatus":"POSTED","timeFrame":"7-21 days post-Device placement","title":"Functionally Adequate Vesico-urethral Anastomosis Within 21 Days Post-Device Placement in Subjects With Successful Device Placement","type":"PRIMARY","unitOfMeasure":"Participants"}