Clinical Research Directory

Inclusion Criteria: * Adult participants, aged 18 years or older * Participant has been indicated for a focal therapy treatment for prostate cancer, radical prostatectomy, or partial nephrectomy robotic procedures * Each participant should fit the clinical criteria to undergo robotic radical procedure, using either the Single Port or Multi Port robotic approaches, laparoscopic, or an open surgical procedure * Each participant should be willing to participate and consent to participate, as documented by a signed informed consent form Exclusion Criteria: * Participants for which minimally invasive surgery is contraindicated as determined by the investigator * Participants with comorbidities or medical characteristics, which would preclude the surgical procedure or the equivalent alternative in the opinion of the investigator * Participants who have been diagnosed with a bleeding disorder and/or cannot be removed from their anticoagulants prior to surgery based on surgeon discretion and standard of care * Non-oncology participants with an estimated life expectancy of less than 6 months * Female participants pregnant at the time of the surgical procedure * Participants who are considered to be part of a vulnerable population, including but not limited to those without sufficient mental capacity * Participants who have participated in an investigational drug or device research study within 30 days of enrollment that would interfere with this study * Participants with active infection including but not limited to pneumonia, urinary tract, cellulitis, or bacteremia