{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","value":"17"}]}],"title":"Known complication: oral hemorrhage"},{"categories":[{"measurements":[{"groupId":"OG000","value":"1"}]}],"title":"Known complication: injury to perioral structures"},{"categories":[{"measurements":[{"groupId":"OG000","value":"14"}]}],"title":"Known complication: airway edema"},{"categories":[{"measurements":[{"groupId":"OG000","value":"1"}]}],"title":"Known complication: nerve injury"},{"categories":[{"measurements":[{"groupId":"OG000","value":"1"}]}],"title":"Need for conversion to open procedure during surge"},{"categories":[{"measurements":[{"groupId":"OG000","value":"11"}]}],"title":"Need for re-exicision due to positive margins"}],"denoms":[{"counts":[{"groupId":"OG000","value":"147"}],"units":"Participants"}],"description":"Assessment of patient safety evaluating the number of participants who experienced known complications from the use of the da Vinci® Robotic System during surgery, who experienced a need for conversion to open surgery during the procedure, or who required additional surgery for re-excision of the lesion due to positive margins","groups":[{"description":"Participants who consented to undergo transoral robotic-assisted surgery using the da Vinci® Robotic System","id":"OG000","title":"TORS Candidates"}],"paramType":"NUMBER","populationDescription":"Participants who successfully underwent transoral robotic-assisted surgery using the da Vinci® Robotic System","reportingStatus":"POSTED","timeFrame":"3 - 24 months postoperatively","title":"Assessment of Patients Safety by Evaluating the Number of Participants Who Experienced Known Complications From the Use of the da Vinci® Robotic System During Surgery, Experienced a Need for Conversion to Open Surgery or Required Additional Surgery.","type":"SECONDARY","unitOfMeasure":"participants"}